Canonical Allele Identifier: CA1335666579

Gene: ATG16L1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233274514_233274515delinsAT , CM000664.2:g.233274514_233274515delinsAT	GRCh38
NC_000002.11:g.234183160_234183161delinsAT , CM000664.1:g.234183160_234183161delinsAT	GRCh37
NC_000002.10:g.233847899_233847900delinsAT	NCBI36
NG_023038.1:g.27944_27945delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392017.9:c.852-162_852-161delinsAT MANE Select	ENSP00000375872.4:n.852-162_852-161delinsAT
ENST00000347464.9:c.363-162_363-161delinsAT	ENSP00000318259.6:n.363-162_363-161delinsAT
ENST00000373525.9:c.420-162_420-161delinsAT	ENSP00000362625.5:n.420-162_420-161delinsAT
ENST00000392017.8:c.852-162_852-161delinsAT	ENSP00000375872.4:n.852-162_852-161delinsAT
ENST00000392018.1:c.903-162_903-161delinsAT	ENSP00000375873.1:n.903-162_903-161delinsAT
ENST00000392020.8:c.795-162_795-161delinsAT	ENSP00000375875.4:n.795-162_795-161delinsAT
ENST00000392021.7:c.*733-162_*733-161delinsAT	ENSP00000375876.3:n.*733-162_*733-161delinsAT
ENST00000419681.5:c.363-162_363-161delinsAT	ENSP00000398773.1:n.363-162_363-161delinsAT
ENST00000444735.5:c.471-162_471-161delinsAT	ENSP00000409215.1:n.471-162_471-161delinsAT
ENST00000474148.5:n.1647-162_1647-161delinsAT
ENST00000479942.5:n.998-162_998-161delinsAT
ENST00000492298.5:n.211_212delinsAT
ENST00000498620.5:n.359-162_359-161delinsAT
NM_001190266.1:c.600-162_600-161delinsAT	NP_001177195.1:n.600-162_600-161delinsAT
NM_001190267.1:c.504-162_504-161delinsAT	NP_001177196.1:n.504-162_504-161delinsAT
NM_017974.3:c.795-162_795-161delinsAT	NP_060444.3:n.795-162_795-161delinsAT
NM_030803.6:c.852-162_852-161delinsAT	NP_110430.5:n.852-162_852-161delinsAT
NM_198890.2:c.363-162_363-161delinsAT	NP_942593.2:n.363-162_363-161delinsAT
XM_005246082.1:c.903-162_903-161delinsAT	XP_005246139.1:n.903-162_903-161delinsAT
XM_005246084.1:c.471-162_471-161delinsAT	XP_005246141.1:n.471-162_471-161delinsAT
XM_005246086.1:c.420-162_420-161delinsAT	XP_005246143.1:n.420-162_420-161delinsAT
XM_006712608.1:c.651-162_651-161delinsAT	XP_006712671.1:n.651-162_651-161delinsAT
XR_241242.1:n.1097-162_1097-161delinsAT
NM_001363742.1:c.903-162_903-161delinsAT	NP_001350671.1:n.903-162_903-161delinsAT
XM_005246084.2:c.471-162_471-161delinsAT	XP_005246141.1:n.471-162_471-161delinsAT
XM_005246086.2:c.420-162_420-161delinsAT	XP_005246143.1:n.420-162_420-161delinsAT
XM_006712608.3:c.651-162_651-161delinsAT	XP_006712671.1:n.651-162_651-161delinsAT
XR_001738801.2:n.1033-162_1033-161delinsAT
XR_241242.3:n.1084-162_1084-161delinsAT
NM_030803.7:c.852-162_852-161delinsAT MANE Select	NP_110430.5:n.852-162_852-161delinsAT
NM_001190266.2:c.600-162_600-161delinsAT	NP_001177195.1:n.600-162_600-161delinsAT
NM_001190267.2:c.504-162_504-161delinsAT	NP_001177196.1:n.504-162_504-161delinsAT
NM_001363742.2:c.903-162_903-161delinsAT	NP_001350671.1:n.903-162_903-161delinsAT
NM_017974.4:c.795-162_795-161delinsAT	NP_060444.3:n.795-162_795-161delinsAT
NM_198890.3:c.363-162_363-161delinsAT	NP_942593.2:n.363-162_363-161delinsAT