Product Details

Assay Reference Genome
Location

Chr.11:46656302 on build GRCh38
Cytoband
11p11.2
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

Target Gene Details

Entrez Gene ID
9776
Gene Symbol
ATG13
Gene Name
autophagy related 13
Gene Aliases
KIAA0652, PARATARG8
Location
Chr.11:46617276-46676019 on build GRCh38
Assay Gene Location
Within Exon 13
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
ATG13 NM_001142673.2 NP_001136145.1
NM_001205119.1 NP_001192048.1
NM_001205120.1 NP_001192049.1
NM_001205121.1 NP_001192050.1
NM_001205122.1 NP_001192051.1
NM_014741.4 NP_055556.2
XM_005253262.2 XP_005253319.1
XM_005253263.2 XP_005253320.1
XM_005253265.2 XP_005253322.1
XM_005253266.2 XP_005253323.1
XM_005253268.2 XP_005253325.1
XM_006718394.2 XP_006718457.1
XM_006718395.2 XP_006718458.1
XM_006718396.2 XP_006718459.1
XM_011520493.1 XP_011518795.1
XM_011520496.2 XP_011518798.1
XM_011520499.2 XP_011518801.1
XM_011520500.1 XP_011518802.1
XM_011520501.1 XP_011518803.1
XM_011520502.1 XP_011518804.1
XM_011520503.1 XP_011518805.1
XM_017018599.1 XP_016874088.1
XM_017018600.1 XP_016874089.1
XM_017018601.1 XP_016874090.1
XM_017018602.1 XP_016874091.1
XM_017018603.1 XP_016874092.1
XM_017018604.1 XP_016874093.1
XM_017018605.1 XP_016874094.1
XM_017018606.1 XP_016874095.1
XM_017018607.1 XP_016874096.1
XM_017018608.1 XP_016874097.1
XM_017018609.1 XP_016874098.1
XM_017018610.1 XP_016874099.1
XM_017018611.1 XP_016874100.1
XM_017018612.1 XP_016874101.1
XM_017018613.1 XP_016874102.1
XM_017018614.1 XP_016874103.1
XM_017018615.1 XP_016874104.1
XM_017018616.1 XP_016874105.1
XM_017018617.1 XP_016874106.1
XM_017018618.1 9 1299 XP_016874107.1
XM_017018619.1 8 1183 XP_016874108.1
XM_017018620.1 8 1243 XP_016874109.1
XM_017018621.1 7 1127 XP_016874110.1
XM_017018622.1 8 1195 XP_016874111.1
AB014552.1
AK023867.1 BAB14707.1
AK223603.1 BAD97323.1
AK289641.1
AK293109.1
AK294110.1
BC001331.1 AAH01331.1
BC002378.2 AAH02378.1
BC006191.2 AAH06191.1
CD675643.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
esv3626191 Chr11:46651662 - 46681651 on Build GRCh38 Gain ATG13 ARHGAP1

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