Canonical Allele Identifier: CA1335666669

Gene: ATG16L1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233274713A= , CM000664.2:g.233274713A=	GRCh38
NC_000002.11:g.234183359A= , CM000664.1:g.234183359A=	GRCh37
NC_000002.10:g.233848098A=	NCBI36
NG_023038.1:g.28143A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392017.9:c.889A= MANE Select	ENSP00000375872.4:p.Asn297=
ENST00000347464.9:c.400A=	ENSP00000318259.6:p.Asn134=
ENST00000373525.9:c.457A=	ENSP00000362625.5:p.Asn153=
ENST00000392017.8:c.889A=	ENSP00000375872.4:p.Asn297=
ENST00000392018.1:c.940A=	ENSP00000375873.1:p.Asn314=
ENST00000392020.8:c.832A=	ENSP00000375875.4:p.Asn278=
ENST00000392021.7:c.*770A=	ENSP00000375876.3:n.*770A=
ENST00000419681.5:c.400A=	ENSP00000398773.1:p.Asn134=
ENST00000444735.5:c.508A=	ENSP00000409215.1:p.Asn170=
ENST00000474148.5:n.1684A=
ENST00000479942.5:n.1035A=
ENST00000492298.5:n.410A=
ENST00000498620.5:n.396A=
NM_001190266.1:c.637A=	NP_001177195.1:p.Asn213=
NM_001190267.1:c.541A=	NP_001177196.1:p.Asn181=
NM_017974.3:c.832A=	NP_060444.3:p.Asn278=
NM_030803.6:c.889A=	NP_110430.5:p.Asn297=
NM_198890.2:c.400A=	NP_942593.2:p.Asn134=
XM_005246082.1:c.940A=	XP_005246139.1:p.Asn314=
XM_005246084.1:c.508A=	XP_005246141.1:p.Asn170=
XM_005246086.1:c.457A=	XP_005246143.1:p.Asn153=
XM_006712608.1:c.688A=	XP_006712671.1:p.Asn230=
XR_241242.1:n.1134A=
NM_001363742.1:c.940A=	NP_001350671.1:p.Asn314=
XM_005246084.2:c.508A=	XP_005246141.1:p.Asn170=
XM_005246086.2:c.457A=	XP_005246143.1:p.Asn153=
XM_006712608.3:c.688A=	XP_006712671.1:p.Asn230=
XR_001738801.2:n.1070A=
XR_241242.3:n.1121A=
NM_030803.7:c.889A= MANE Select	NP_110430.5:p.Asn297=
NM_001190266.2:c.637A=	NP_001177195.1:p.Asn213=
NM_001190267.2:c.541A=	NP_001177196.1:p.Asn181=
NM_001363742.2:c.940A=	NP_001350671.1:p.Asn314=
NM_017974.4:c.832A=	NP_060444.3:p.Asn278=
NM_198890.3:c.400A=	NP_942593.2:p.Asn134=