Product Details

Primer Sequences: Log in to view
Primer Chromosome Location: Chr.12: 2120264-2120489 on Build GRCh38 View in UCSC browser
Format: Each primer will be delivered in a single tube, dried-down
Quick Reference Guide: Primer Designer^™ Tool Quick Reference
Ampliseq ID's

Gene Details

Gene Symbol: CACNA1C
Entrez Gene ID: 775
Gene Name: calcium voltage-gated channel subunit alpha1 C
Gene Aliases: CACH2, CACN2, CACNL1A1, CCHL1A1, CaV1.2, LQT8, TS
UniGene: Hs.118262
Gene Chromosome Location: Chr.12: 1969677-2697949 on Build GRCh38
Transcripts: NM_000719.6 NM_001129827.1 NM_001129829.1 NM_001129830.2 NM_001129831.1 NM_001129832.1 NM_001129833.1 NM_001129834.1 NM_001129835.1 NM_001129836.1 NM_001129837.1 NM_001129838.1 NM_001129839.1 NM_001129840.1 NM_001129841.1 NM_001129842.1 NM_001129843.1 NM_001129844.1 NM_001129846.1 NM_001167623.1 NM_001167624.2 NM_001167625.1 NM_199460.3 XM_006719017.2 XM_011521020.2 XM_011521023.2 XM_017019926.1 XM_017019927.1 XM_017019928.1 XM_017019929.1 XM_017019930.1 XM_017019931.1 XM_017019932.1 XM_017019933.1 XM_017019934.1 XM_017019935.1 XM_017019936.1 XM_017019937.1 XM_017019938.1 XM_017019939.1 XM_017019940.1 XM_017019941.1 XM_017019942.1 XM_017019943.1 XM_017019944.1 XM_017019945.1 XM_017019946.1 XM_017019947.1 XM_017019948.1 XM_017019949.1 XM_017019950.1 XM_017019951.1 XM_017019952.1 XM_017019953.1 XM_017019954.1 XM_017019955.1

Cosmic Detail

Cosmic ID	Mutation	AA	Transcript Location
3459417	c.443C>T	p.P148L	Chr.12: 2120396-2120396 on Build GRCh38
3739563	c.408C>A	p.A136A	Chr.12: 2120361-2120361 on Build GRCh38
3739566	c.498C>A	p.A166A	Chr.12: 2120361-2120361 on Build GRCh38
3739564	c.408C>A	p.A136A	Chr.12: 2120361-2120361 on Build GRCh38
6617626	c.394C>T	p.L132L	Chr.12: 2120347-2120347 on Build GRCh38
2005633	c.460G>A	p.A154T	Chr.12: 2120413-2120413 on Build GRCh38
6577138	c.422T>C	p.L141S	Chr.12: 2120375-2120375 on Build GRCh38
397445	c.374C>A	p.P125Q	Chr.12: 2120327-2120327 on Build GRCh38
4547249	c.418G>A	p.A140T	Chr.12: 2120371-2120371 on Build GRCh38
397446	c.464C>A	p.P155Q	Chr.12: 2120327-2120327 on Build GRCh38
4806824	c.477T>G	p.I159M	Chr.12: 2120340-2120340 on Build GRCh38
2005627	c.549C>T	p.N183N	Chr.12: 2120412-2120412 on Build GRCh38
6617624	c.394C>T	p.L132L	Chr.12: 2120347-2120347 on Build GRCh38
4547247	c.418G>A	p.A140T	Chr.12: 2120371-2120371 on Build GRCh38
1736399	c.413G>T	p.C138F	Chr.12: 2120366-2120366 on Build GRCh38
3459414	c.443C>T	p.P148L	Chr.12: 2120396-2120396 on Build GRCh38
2005631	c.460G>A	p.A154T	Chr.12: 2120413-2120413 on Build GRCh38
2005615	c.419C>T	p.A140V	Chr.12: 2120372-2120372 on Build GRCh38
2005616	c.419C>T	p.A140V	Chr.12: 2120372-2120372 on Build GRCh38
4806823	c.387T>G	p.I129M	Chr.12: 2120340-2120340 on Build GRCh38
3459416	c.533C>T	p.P178L	Chr.12: 2120396-2120396 on Build GRCh38
7123025	c.448G>T	p.D150Y	Chr.12: 2120401-2120401 on Build GRCh38
4911505	c.477G>T	p.L159L	Chr.12: 2120430-2120430 on Build GRCh38
7123022	c.538G>T	p.D180Y	Chr.12: 2120401-2120401 on Build GRCh38
2005630	c.460G>A	p.A154T	Chr.12: 2120413-2120413 on Build GRCh38
2005614	c.419C>T	p.A140V	Chr.12: 2120372-2120372 on Build GRCh38
2005628	c.459C>T	p.N153N	Chr.12: 2120412-2120412 on Build GRCh38
1736402	c.413G>T	p.C138F	Chr.12: 2120366-2120366 on Build GRCh38
3459413	c.443C>T	p.P148L	Chr.12: 2120396-2120396 on Build GRCh38
4911502	c.477G>T	p.L159L	Chr.12: 2120430-2120430 on Build GRCh38
2005629	c.460G>A	p.A154T	Chr.12: 2120413-2120413 on Build GRCh38
4911503	c.477G>T	p.L159L	Chr.12: 2120430-2120430 on Build GRCh38
6617627	c.484C>T	p.L162L	Chr.12: 2120347-2120347 on Build GRCh38
7123026	c.448G>T	p.D150Y	Chr.12: 2120401-2120401 on Build GRCh38
4547248	c.508G>A	p.A170T	Chr.12: 2120371-2120371 on Build GRCh38
4806822	c.387T>G	p.I129M	Chr.12: 2120340-2120340 on Build GRCh38
4911501	c.477G>T	p.L159L	Chr.12: 2120430-2120430 on Build GRCh38
4547246	c.418G>A	p.A140T	Chr.12: 2120371-2120371 on Build GRCh38
1736401	c.503G>T	p.C168F	Chr.12: 2120366-2120366 on Build GRCh38
6577140	c.512T>C	p.L171S	Chr.12: 2120375-2120375 on Build GRCh38
2005617	c.509C>T	p.A170V	Chr.12: 2120372-2120372 on Build GRCh38
1736400	c.413G>T	p.C138F	Chr.12: 2120366-2120366 on Build GRCh38
3739567	c.408C>A	p.A136A	Chr.12: 2120361-2120361 on Build GRCh38
7123024	c.448G>T	p.D150Y	Chr.12: 2120401-2120401 on Build GRCh38
2005626	c.459C>T	p.N153N	Chr.12: 2120412-2120412 on Build GRCh38
6617628	c.394C>T	p.L132L	Chr.12: 2120347-2120347 on Build GRCh38
2005632	c.550G>A	p.A184T	Chr.12: 2120413-2120413 on Build GRCh38
1736398	c.413G>T	p.C138F	Chr.12: 2120366-2120366 on Build GRCh38
4806821	c.387T>G	p.I129M	Chr.12: 2120340-2120340 on Build GRCh38
2005625	c.459C>T	p.N153N	Chr.12: 2120412-2120412 on Build GRCh38
6577139	c.422T>C	p.L141S	Chr.12: 2120375-2120375 on Build GRCh38
3459415	c.443C>T	p.P148L	Chr.12: 2120396-2120396 on Build GRCh38
4547245	c.418G>A	p.A140T	Chr.12: 2120371-2120371 on Build GRCh38
4806825	c.387T>G	p.I129M	Chr.12: 2120340-2120340 on Build GRCh38
6577137	c.422T>C	p.L141S	Chr.12: 2120375-2120375 on Build GRCh38
2005618	c.419C>T	p.A140V	Chr.12: 2120372-2120372 on Build GRCh38
4911504	c.567G>T	p.L189L	Chr.12: 2120430-2120430 on Build GRCh38
3739565	c.408C>A	p.A136A	Chr.12: 2120361-2120361 on Build GRCh38
6577141	c.422T>C	p.L141S	Chr.12: 2120375-2120375 on Build GRCh38
7123023	c.448G>T	p.D150Y	Chr.12: 2120401-2120401 on Build GRCh38
2005624	c.459C>T	p.N153N	Chr.12: 2120412-2120412 on Build GRCh38
6617625	c.394C>T	p.L132L	Chr.12: 2120347-2120347 on Build GRCh38

SNP Detail

SNP ID	Chromosome Location
rs751407951	Chr.12: 2120449-2120449 on Build GRCh38
rs546786746	Chr.12: 2120379-2120379 on Build GRCh38
rs186692112	Chr.12: 2120467-2120467 on Build GRCh38
rs761891438	Chr.12: 2120300-2120300 on Build GRCh38
rs367638447	Chr.12: 2120412-2120412 on Build GRCh38
rs375212916	Chr.12: 2120296-2120296 on Build GRCh38
rs772557072	Chr.12: 2120373-2120373 on Build GRCh38
rs747719890	Chr.12: 2120360-2120360 on Build GRCh38
rs748949538	Chr.12: 2120372-2120372 on Build GRCh38
rs760538776	Chr.12: 2120297-2120297 on Build GRCh38
rs776532518	Chr.12: 2120409-2120409 on Build GRCh38
rs780660896	Chr.12: 2120350-2120350 on Build GRCh38
rs763228787	Chr.12: 2120438-2120438 on Build GRCh38
rs367763190	Chr.12: 2120316-2120316 on Build GRCh38
rs55792866	Chr.12: 2120310-2120310 on Build GRCh38
rs754865091	Chr.12: 2120453-2120453 on Build GRCh38
rs961457767	Chr.12: 2120437-2120437 on Build GRCh38
rs769308149	Chr.12: 2120397-2120397 on Build GRCh38
rs769295096	Chr.12: 2120361-2120361 on Build GRCh38
rs750120212	Chr.12: 2120306-2120306 on Build GRCh38
rs533097898	Chr.12: 2120367-2120367 on Build GRCh38
rs587780882	Chr.12: 2120328-2120328 on Build GRCh38
rs750645940	Chr.12: 2120416-2120416 on Build GRCh38
rs761958170	Chr.12: 2120411-2120411 on Build GRCh38
rs200282707	Chr.12: 2120302-2120302 on Build GRCh38
rs1019342847	Chr.12: 2120427-2120427 on Build GRCh38
rs761239778	Chr.12: 2120384-2120384 on Build GRCh38
rs371836468	Chr.12: 2120444-2120444 on Build GRCh38
rs754951873	Chr.12: 2120335-2120335 on Build GRCh38

View Full Product Details