Canonical Allele Identifier: CA1335666647
Gene: ATG16L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233274658_233274660delinsCTT , CM000664.2:g.233274658_233274660delinsCTT GRCh38
NC_000002.11:g.234183304_234183306delinsCTT , CM000664.1:g.234183304_234183306delinsCTT GRCh37
NC_000002.10:g.233848043_233848045delinsCTT NCBI36
NG_023038.1:g.28088_28090delinsCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000392017.9:c.852-18_852-16delinsCTT MANE Select ENSP00000375872.4:n.852-18_852-16delinsCTT
ENST00000347464.9:c.363-18_363-16delinsCTT ENSP00000318259.6:n.363-18_363-16delinsCTT
ENST00000373525.9:c.420-18_420-16delinsCTT ENSP00000362625.5:n.420-18_420-16delinsCTT
ENST00000392017.8:c.852-18_852-16delinsCTT ENSP00000375872.4:n.852-18_852-16delinsCTT
ENST00000392018.1:c.903-18_903-16delinsCTT ENSP00000375873.1:n.903-18_903-16delinsCTT
ENST00000392020.8:c.795-18_795-16delinsCTT ENSP00000375875.4:n.795-18_795-16delinsCTT
ENST00000392021.7:c.*733-18_*733-16delinsCTT ENSP00000375876.3:n.*733-18_*733-16delinsCTT
ENST00000419681.5:c.363-18_363-16delinsCTT ENSP00000398773.1:n.363-18_363-16delinsCTT
ENST00000444735.5:c.471-18_471-16delinsCTT ENSP00000409215.1:n.471-18_471-16delinsCTT
ENST00000474148.5:n.1647-18_1647-16delinsCTT
ENST00000479942.5:n.998-18_998-16delinsCTT
ENST00000492298.5:n.355_357delinsCTT
ENST00000498620.5:n.359-18_359-16delinsCTT
NM_001190266.1:c.600-18_600-16delinsCTT NP_001177195.1:n.600-18_600-16delinsCTT
NM_001190267.1:c.504-18_504-16delinsCTT NP_001177196.1:n.504-18_504-16delinsCTT
NM_017974.3:c.795-18_795-16delinsCTT NP_060444.3:n.795-18_795-16delinsCTT
NM_030803.6:c.852-18_852-16delinsCTT NP_110430.5:n.852-18_852-16delinsCTT
NM_198890.2:c.363-18_363-16delinsCTT NP_942593.2:n.363-18_363-16delinsCTT
XM_005246082.1:c.903-18_903-16delinsCTT XP_005246139.1:n.903-18_903-16delinsCTT
XM_005246084.1:c.471-18_471-16delinsCTT XP_005246141.1:n.471-18_471-16delinsCTT
XM_005246086.1:c.420-18_420-16delinsCTT XP_005246143.1:n.420-18_420-16delinsCTT
XM_006712608.1:c.651-18_651-16delinsCTT XP_006712671.1:n.651-18_651-16delinsCTT
XR_241242.1:n.1097-18_1097-16delinsCTT
NM_001363742.1:c.903-18_903-16delinsCTT NP_001350671.1:n.903-18_903-16delinsCTT
XM_005246084.2:c.471-18_471-16delinsCTT XP_005246141.1:n.471-18_471-16delinsCTT
XM_005246086.2:c.420-18_420-16delinsCTT XP_005246143.1:n.420-18_420-16delinsCTT
XM_006712608.3:c.651-18_651-16delinsCTT XP_006712671.1:n.651-18_651-16delinsCTT
XR_001738801.2:n.1033-18_1033-16delinsCTT
XR_241242.3:n.1084-18_1084-16delinsCTT
NM_030803.7:c.852-18_852-16delinsCTT MANE Select NP_110430.5:n.852-18_852-16delinsCTT
NM_001190266.2:c.600-18_600-16delinsCTT NP_001177195.1:n.600-18_600-16delinsCTT
NM_001190267.2:c.504-18_504-16delinsCTT NP_001177196.1:n.504-18_504-16delinsCTT
NM_001363742.2:c.903-18_903-16delinsCTT NP_001350671.1:n.903-18_903-16delinsCTT
NM_017974.4:c.795-18_795-16delinsCTT NP_060444.3:n.795-18_795-16delinsCTT
NM_198890.3:c.363-18_363-16delinsCTT NP_942593.2:n.363-18_363-16delinsCTT