Canonical Allele Identifier: CA1335666675
Gene: ATG16L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233274728C= , CM000664.2:g.233274728C= GRCh38
NC_000002.11:g.234183374C= , CM000664.1:g.234183374C= GRCh37
NC_000002.10:g.233848113C= NCBI36
NG_023038.1:g.28158C=

Transcript Alleles

HGVS Amino-acid change
ENST00000392017.9:c.904C= MANE Select ENSP00000375872.4:p.Pro302=
ENST00000347464.9:c.415C= ENSP00000318259.6:p.Pro139=
ENST00000373525.9:c.472C= ENSP00000362625.5:p.Pro158=
ENST00000392017.8:c.904C= ENSP00000375872.4:p.Pro302=
ENST00000392018.1:c.955C= ENSP00000375873.1:p.Pro319=
ENST00000392020.8:c.847C= ENSP00000375875.4:p.Pro283=
ENST00000392021.7:c.*785C= ENSP00000375876.3:n.*785C=
ENST00000419681.5:c.415C= ENSP00000398773.1:p.Pro139=
ENST00000444735.5:c.523C= ENSP00000409215.1:p.Pro175=
ENST00000474148.5:n.1699C=
ENST00000479942.5:n.1050C=
ENST00000492298.5:n.425C=
ENST00000498620.5:n.411C=
NM_001190266.1:c.652C= NP_001177195.1:p.Pro218=
NM_001190267.1:c.556C= NP_001177196.1:p.Pro186=
NM_017974.3:c.847C= NP_060444.3:p.Pro283=
NM_030803.6:c.904C= NP_110430.5:p.Pro302=
NM_198890.2:c.415C= NP_942593.2:p.Pro139=
XM_005246082.1:c.955C= XP_005246139.1:p.Pro319=
XM_005246084.1:c.523C= XP_005246141.1:p.Pro175=
XM_005246086.1:c.472C= XP_005246143.1:p.Pro158=
XM_006712608.1:c.703C= XP_006712671.1:p.Pro235=
XR_241242.1:n.1149C=
NM_001363742.1:c.955C= NP_001350671.1:p.Pro319=
XM_005246084.2:c.523C= XP_005246141.1:p.Pro175=
XM_005246086.2:c.472C= XP_005246143.1:p.Pro158=
XM_006712608.3:c.703C= XP_006712671.1:p.Pro235=
XR_001738801.2:n.1085C=
XR_241242.3:n.1136C=
NM_030803.7:c.904C= MANE Select NP_110430.5:p.Pro302=
NM_001190266.2:c.652C= NP_001177195.1:p.Pro218=
NM_001190267.2:c.556C= NP_001177196.1:p.Pro186=
NM_001363742.2:c.955C= NP_001350671.1:p.Pro319=
NM_017974.4:c.847C= NP_060444.3:p.Pro283=
NM_198890.3:c.415C= NP_942593.2:p.Pro139=