Canonical Allele Identifier: CA1335666655

Gene: ATG16L1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233274679A= , CM000664.2:g.233274679A=	GRCh38
NC_000002.11:g.234183325A= , CM000664.1:g.234183325A=	GRCh37
NC_000002.10:g.233848064A=	NCBI36
NG_023038.1:g.28109A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392017.9:c.855A= MANE Select	ENSP00000375872.4:p.Arg285=
ENST00000347464.9:c.366A=	ENSP00000318259.6:p.Arg122=
ENST00000373525.9:c.423A=	ENSP00000362625.5:p.Arg141=
ENST00000392017.8:c.855A=	ENSP00000375872.4:p.Arg285=
ENST00000392018.1:c.906A=	ENSP00000375873.1:p.Arg302=
ENST00000392020.8:c.798A=	ENSP00000375875.4:p.Arg266=
ENST00000392021.7:c.*736A=	ENSP00000375876.3:n.*736A=
ENST00000419681.5:c.366A=	ENSP00000398773.1:p.Arg122=
ENST00000444735.5:c.474A=	ENSP00000409215.1:p.Arg158=
ENST00000474148.5:n.1650A=
ENST00000479942.5:n.1001A=
ENST00000492298.5:n.376A=
ENST00000498620.5:n.362A=
NM_001190266.1:c.603A=	NP_001177195.1:p.Arg201=
NM_001190267.1:c.507A=	NP_001177196.1:p.Arg169=
NM_017974.3:c.798A=	NP_060444.3:p.Arg266=
NM_030803.6:c.855A=	NP_110430.5:p.Arg285=
NM_198890.2:c.366A=	NP_942593.2:p.Arg122=
XM_005246082.1:c.906A=	XP_005246139.1:p.Arg302=
XM_005246084.1:c.474A=	XP_005246141.1:p.Arg158=
XM_005246086.1:c.423A=	XP_005246143.1:p.Arg141=
XM_006712608.1:c.654A=	XP_006712671.1:p.Arg218=
XR_241242.1:n.1100A=
NM_001363742.1:c.906A=	NP_001350671.1:p.Arg302=
XM_005246084.2:c.474A=	XP_005246141.1:p.Arg158=
XM_005246086.2:c.423A=	XP_005246143.1:p.Arg141=
XM_006712608.3:c.654A=	XP_006712671.1:p.Arg218=
XR_001738801.2:n.1036A=
XR_241242.3:n.1087A=
NM_030803.7:c.855A= MANE Select	NP_110430.5:p.Arg285=
NM_001190266.2:c.603A=	NP_001177195.1:p.Arg201=
NM_001190267.2:c.507A=	NP_001177196.1:p.Arg169=
NM_001363742.2:c.906A=	NP_001350671.1:p.Arg302=
NM_017974.4:c.798A=	NP_060444.3:p.Arg266=
NM_198890.3:c.366A=	NP_942593.2:p.Arg122=