Product Details

Primer Sequences

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Primer Chromosome Location

Chr.11: 113205988-113206239 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

NCAM1

Entrez Gene ID

4684

Gene Name

neural cell adhesion molecule 1

Gene Aliases

CD56, MSK39, NCAM

UniGene

Hs.503878

Gene Chromosome Location

Chr.11: 112961247-113278436 on Build GRCh38

Transcripts

NM_000615.6 NM_001076682.3 NM_001242607.1 NM_001242608.1 NM_181351.4

Cosmic Detail

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Cosmic ID	Mutation	AA	Transcript Location
4902868	c.570C>A	p.G190G	Chr.11: 113206125-113206125 on Build GRCh38
428423	c.547G>A	p.E183K	Chr.11: 113206102-113206102 on Build GRCh38
3443435	c.562G>A	p.E188K	Chr.11: 113206144-113206144 on Build GRCh38
1475042	c.525C>T	p.I175I	Chr.11: 113206080-113206080 on Build GRCh38
5535236	c.615C>T	p.V205V	Chr.11: 113206170-113206170 on Build GRCh38
5882002	c.541G>T	p.G181C	Chr.11: 113206123-113206123 on Build GRCh38
2102920	c.464G>A	p.R155Q	Chr.11: 113206046-113206046 on Build GRCh38
1258771	c.583_584insG	p.E197fs*64	Chr.11: 113206138-113206139 on Build GRCh38
5129139	c.500delG	p.G168fs*31	Chr.11: 113206082-113206082 on Build GRCh38
5176687	c.583C>T	p.R195W	Chr.11: 113206138-113206138 on Build GRCh38
5882003	c.568G>T	p.G190C	Chr.11: 113206123-113206123 on Build GRCh38
7185508	c.524G>A	p.G175D	Chr.11: 113206106-113206106 on Build GRCh38
3443437	c.589G>A	p.E197K	Chr.11: 113206144-113206144 on Build GRCh38
428421	c.520G>A	p.E174K	Chr.11: 113206102-113206102 on Build GRCh38
1351303	c.500G>A	p.R167Q	Chr.11: 113206082-113206082 on Build GRCh38
6722582	c.522G>T	p.E174D	Chr.11: 113206104-113206104 on Build GRCh38
6865180	c.510C>T	p.N170N	Chr.11: 113206065-113206065 on Build GRCh38
6997380	c.562delG	p.E188fs*11	Chr.11: 113206144-113206144 on Build GRCh38
5535234	c.588C>T	p.V196V	Chr.11: 113206170-113206170 on Build GRCh38
6997382	c.589delG	p.E197fs*11	Chr.11: 113206144-113206144 on Build GRCh38
2102919	c.490C>T	p.R164*	Chr.11: 113206045-113206045 on Build GRCh38
5129141	c.527delG	p.G177fs*31	Chr.11: 113206082-113206082 on Build GRCh38
5579051	c.499C>G	p.R167G	Chr.11: 113206081-113206081 on Build GRCh38
6067333	c.474C>A	p.V158V	Chr.11: 113206056-113206056 on Build GRCh38
352333	c.495G>T	p.Q165H	Chr.11: 113206077-113206077 on Build GRCh38
1475041	c.498C>T	p.I166I	Chr.11: 113206080-113206080 on Build GRCh38
352335	c.522G>T	p.Q174H	Chr.11: 113206077-113206077 on Build GRCh38
5579052	c.526C>G	p.R176G	Chr.11: 113206081-113206081 on Build GRCh38
5581811	c.577C>T	p.L193L	Chr.11: 113206132-113206132 on Build GRCh38
4553988	c.604G>A	p.D202N	Chr.11: 113206159-113206159 on Build GRCh38
923120	c.582T>C	p.I194I	Chr.11: 113206164-113206164 on Build GRCh38
4902866	c.543C>A	p.G181G	Chr.11: 113206125-113206125 on Build GRCh38
4184414	c.544G>A	p.D182N	Chr.11: 113206099-113206099 on Build GRCh38
6722584	c.549G>T	p.E183D	Chr.11: 113206104-113206104 on Build GRCh38
4410924	c.499C>T	p.R167W	Chr.11: 113206081-113206081 on Build GRCh38
6067334	c.501C>A	p.V167V	Chr.11: 113206056-113206056 on Build GRCh38
4410925	c.526C>T	p.R176W	Chr.11: 113206081-113206081 on Build GRCh38
6419789	c.489C>A	p.V163V	Chr.11: 113206044-113206044 on Build GRCh38
7185510	c.551G>A	p.G184D	Chr.11: 113206106-113206106 on Build GRCh38
4017865	c.588G>A	p.G196G	Chr.11: 113206143-113206143 on Build GRCh38
4184413	c.517G>A	p.D173N	Chr.11: 113206099-113206099 on Build GRCh38
341639	c.480C>A	p.S160S	Chr.11: 113206062-113206062 on Build GRCh38
1351304	c.527G>A	p.R176Q	Chr.11: 113206082-113206082 on Build GRCh38
5176685	c.556C>T	p.R186W	Chr.11: 113206138-113206138 on Build GRCh38
5040670	c.593T>A	p.V198E	Chr.11: 113206175-113206175 on Build GRCh38
6865178	c.483C>T	p.N161N	Chr.11: 113206065-113206065 on Build GRCh38
341641	c.507C>A	p.S169S	Chr.11: 113206062-113206062 on Build GRCh38
1258770	c.556_557insG	p.E188fs*64	Chr.11: 113206138-113206139 on Build GRCh38
2102922	c.491G>A	p.R164Q	Chr.11: 113206046-113206046 on Build GRCh38
5581810	c.550C>T	p.L184L	Chr.11: 113206132-113206132 on Build GRCh38
2102917	c.463C>T	p.R155*	Chr.11: 113206045-113206045 on Build GRCh38
4017863	c.561G>A	p.G187G	Chr.11: 113206143-113206143 on Build GRCh38
4553987	c.577G>A	p.D193N	Chr.11: 113206159-113206159 on Build GRCh38
5040672	c.620T>A	p.V207E	Chr.11: 113206175-113206175 on Build GRCh38
923122	c.609T>C	p.I203I	Chr.11: 113206164-113206164 on Build GRCh38
6419788	c.462C>A	p.V154V	Chr.11: 113206044-113206044 on Build GRCh38

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SNP Detail

SNP ID	Chromosome Location
rs781929864	Chr.11: 113206188-113206188 on Build GRCh38
rs782535732	Chr.11: 113206091-113206091 on Build GRCh38
rs377417619	Chr.11: 113206194-113206194 on Build GRCh38
rs782517960	Chr.11: 113206203-113206203 on Build GRCh38
rs782014259	Chr.11: 113206146-113206146 on Build GRCh38
rs782242910	Chr.11: 113206136-113206136 on Build GRCh38
rs35576001	Chr.11: 113206082-113206082 on Build GRCh38
rs576548045	Chr.11: 113206138-113206138 on Build GRCh38
rs556599914	Chr.11: 113206097-113206097 on Build GRCh38
rs782807183	Chr.11: 113206016-113206016 on Build GRCh38
rs949627474	Chr.11: 113206156-113206156 on Build GRCh38
rs782184114	Chr.11: 113206105-113206105 on Build GRCh38
rs376708434	Chr.11: 113206115-113206115 on Build GRCh38
rs781819663	Chr.11: 113206043-113206043 on Build GRCh38
rs369920955	Chr.11: 113206193-113206193 on Build GRCh38
rs559320851	Chr.11: 113206200-113206200 on Build GRCh38
rs782683789	Chr.11: 113206183-113206183 on Build GRCh38
rs782161510	Chr.11: 113206165-113206165 on Build GRCh38
rs782579837	Chr.11: 113206039-113206039 on Build GRCh38
rs782494134	Chr.11: 113206056-113206056 on Build GRCh38
rs782329784	Chr.11: 113206109-113206109 on Build GRCh38
rs782813348	Chr.11: 113206206-113206206 on Build GRCh38
rs782525915	Chr.11: 113206022-113206022 on Build GRCh38
rs782632084	Chr.11: 113206081-113206081 on Build GRCh38

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