Canonical Allele Identifier: CA1335666668

Gene: ATG16L1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233274711A= , CM000664.2:g.233274711A=	GRCh38
NC_000002.11:g.234183357A= , CM000664.1:g.234183357A=	GRCh37
NC_000002.10:g.233848096A=	NCBI36
NG_023038.1:g.28141A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392017.9:c.887A= MANE Select	ENSP00000375872.4:p.Asp296=
ENST00000347464.9:c.398A=	ENSP00000318259.6:p.Asp133=
ENST00000373525.9:c.455A=	ENSP00000362625.5:p.Asp152=
ENST00000392017.8:c.887A=	ENSP00000375872.4:p.Asp296=
ENST00000392018.1:c.938A=	ENSP00000375873.1:p.Asp313=
ENST00000392020.8:c.830A=	ENSP00000375875.4:p.Asp277=
ENST00000392021.7:c.*768A=	ENSP00000375876.3:n.*768A=
ENST00000419681.5:c.398A=	ENSP00000398773.1:p.Asp133=
ENST00000444735.5:c.506A=	ENSP00000409215.1:p.Asp169=
ENST00000474148.5:n.1682A=
ENST00000479942.5:n.1033A=
ENST00000492298.5:n.408A=
ENST00000498620.5:n.394A=
NM_001190266.1:c.635A=	NP_001177195.1:p.Asp212=
NM_001190267.1:c.539A=	NP_001177196.1:p.Asp180=
NM_017974.3:c.830A=	NP_060444.3:p.Asp277=
NM_030803.6:c.887A=	NP_110430.5:p.Asp296=
NM_198890.2:c.398A=	NP_942593.2:p.Asp133=
XM_005246082.1:c.938A=	XP_005246139.1:p.Asp313=
XM_005246084.1:c.506A=	XP_005246141.1:p.Asp169=
XM_005246086.1:c.455A=	XP_005246143.1:p.Asp152=
XM_006712608.1:c.686A=	XP_006712671.1:p.Asp229=
XR_241242.1:n.1132A=
NM_001363742.1:c.938A=	NP_001350671.1:p.Asp313=
XM_005246084.2:c.506A=	XP_005246141.1:p.Asp169=
XM_005246086.2:c.455A=	XP_005246143.1:p.Asp152=
XM_006712608.3:c.686A=	XP_006712671.1:p.Asp229=
XR_001738801.2:n.1068A=
XR_241242.3:n.1119A=
NM_030803.7:c.887A= MANE Select	NP_110430.5:p.Asp296=
NM_001190266.2:c.635A=	NP_001177195.1:p.Asp212=
NM_001190267.2:c.539A=	NP_001177196.1:p.Asp180=
NM_001363742.2:c.938A=	NP_001350671.1:p.Asp313=
NM_017974.4:c.830A=	NP_060444.3:p.Asp277=
NM_198890.3:c.398A=	NP_942593.2:p.Asp133=