Canonical Allele Identifier: CA1335666632
Gene: ATG16L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233274632_233274634delinsCCT , CM000664.2:g.233274632_233274634delinsCCT GRCh38
NC_000002.11:g.234183278_234183280delinsCCT , CM000664.1:g.234183278_234183280delinsCCT GRCh37
NC_000002.10:g.233848017_233848019delinsCCT NCBI36
NG_023038.1:g.28062_28064delinsCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000392017.9:c.852-44_852-42delinsCCT MANE Select ENSP00000375872.4:n.852-44_852-42delinsCC...
ENST00000347464.9:c.363-44_363-42delinsCCT ENSP00000318259.6:n.363-44_363-42delinsCC...
ENST00000373525.9:c.420-44_420-42delinsCCT ENSP00000362625.5:n.420-44_420-42delinsCC...
ENST00000392017.8:c.852-44_852-42delinsCCT ENSP00000375872.4:n.852-44_852-42delinsCC...
ENST00000392018.1:c.903-44_903-42delinsCCT ENSP00000375873.1:n.903-44_903-42delinsCC...
ENST00000392020.8:c.795-44_795-42delinsCCT ENSP00000375875.4:n.795-44_795-42delinsCC...
ENST00000392021.7:c.*733-44_*733-42delinsCCT ENSP00000375876.3:n.*733-44_*733-42delins...
ENST00000419681.5:c.363-44_363-42delinsCCT ENSP00000398773.1:n.363-44_363-42delinsCC...
ENST00000444735.5:c.471-44_471-42delinsCCT ENSP00000409215.1:n.471-44_471-42delinsCC...
ENST00000474148.5:n.1647-44_1647-42delinsCCT
ENST00000479942.5:n.998-44_998-42delinsCCT
ENST00000492298.5:n.329_331delinsCCT
ENST00000498620.5:n.359-44_359-42delinsCCT
NM_001190266.1:c.600-44_600-42delinsCCT NP_001177195.1:n.600-44_600-42delinsCCT
NM_001190267.1:c.504-44_504-42delinsCCT NP_001177196.1:n.504-44_504-42delinsCCT
NM_017974.3:c.795-44_795-42delinsCCT NP_060444.3:n.795-44_795-42delinsCCT
NM_030803.6:c.852-44_852-42delinsCCT NP_110430.5:n.852-44_852-42delinsCCT
NM_198890.2:c.363-44_363-42delinsCCT NP_942593.2:n.363-44_363-42delinsCCT
XM_005246082.1:c.903-44_903-42delinsCCT XP_005246139.1:n.903-44_903-42delinsCCT
XM_005246084.1:c.471-44_471-42delinsCCT XP_005246141.1:n.471-44_471-42delinsCCT
XM_005246086.1:c.420-44_420-42delinsCCT XP_005246143.1:n.420-44_420-42delinsCCT
XM_006712608.1:c.651-44_651-42delinsCCT XP_006712671.1:n.651-44_651-42delinsCCT
XR_241242.1:n.1097-44_1097-42delinsCCT
NM_001363742.1:c.903-44_903-42delinsCCT NP_001350671.1:n.903-44_903-42delinsCCT
XM_005246084.2:c.471-44_471-42delinsCCT XP_005246141.1:n.471-44_471-42delinsCCT
XM_005246086.2:c.420-44_420-42delinsCCT XP_005246143.1:n.420-44_420-42delinsCCT
XM_006712608.3:c.651-44_651-42delinsCCT XP_006712671.1:n.651-44_651-42delinsCCT
XR_001738801.2:n.1033-44_1033-42delinsCCT
XR_241242.3:n.1084-44_1084-42delinsCCT
NM_030803.7:c.852-44_852-42delinsCCT MANE Select NP_110430.5:n.852-44_852-42delinsCCT
NM_001190266.2:c.600-44_600-42delinsCCT NP_001177195.1:n.600-44_600-42delinsCCT
NM_001190267.2:c.504-44_504-42delinsCCT NP_001177196.1:n.504-44_504-42delinsCCT
NM_001363742.2:c.903-44_903-42delinsCCT NP_001350671.1:n.903-44_903-42delinsCCT
NM_017974.4:c.795-44_795-42delinsCCT NP_060444.3:n.795-44_795-42delinsCCT
NM_198890.3:c.363-44_363-42delinsCCT NP_942593.2:n.363-44_363-42delinsCCT