Canonical Allele Identifier: CA1335666764

Gene: ATG16L1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233274929T= , CM000664.2:g.233274929T=	GRCh38
NC_000002.11:g.234183575T= , CM000664.1:g.234183575T=	GRCh37
NC_000002.10:g.233848314T=	NCBI36
NG_023038.1:g.28359T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392017.9:c.954+151T= MANE Select	ENSP00000375872.4:n.954+151T=
ENST00000347464.9:c.465+151T=	ENSP00000318259.6:n.465+151T=
ENST00000373525.9:c.522+151T=	ENSP00000362625.5:n.522+151T=
ENST00000392017.8:c.954+151T=	ENSP00000375872.4:n.954+151T=
ENST00000392018.1:c.1005+151T=	ENSP00000375873.1:n.1005+151T=
ENST00000392020.8:c.897+151T=	ENSP00000375875.4:n.897+151T=
ENST00000392021.7:c.*835+151T=	ENSP00000375876.3:n.*835+151T=
ENST00000419681.5:c.465+151T=	ENSP00000398773.1:n.465+151T=
ENST00000474148.5:n.1749+151T=
ENST00000479942.5:n.1100+151T=
ENST00000492298.5:n.475+151T=
ENST00000498620.5:n.461+151T=
NM_001190266.1:c.702+151T=	NP_001177195.1:n.702+151T=
NM_001190267.1:c.606+151T=	NP_001177196.1:n.606+151T=
NM_017974.3:c.897+151T=	NP_060444.3:n.897+151T=
NM_030803.6:c.954+151T=	NP_110430.5:n.954+151T=
NM_198890.2:c.465+151T=	NP_942593.2:n.465+151T=
XM_005246082.1:c.1005+151T=	XP_005246139.1:n.1005+151T=
XM_005246084.1:c.573+151T=	XP_005246141.1:n.573+151T=
XM_005246086.1:c.522+151T=	XP_005246143.1:n.522+151T=
XM_006712608.1:c.753+151T=	XP_006712671.1:n.753+151T=
XR_241242.1:n.1199+151T=
NM_001363742.1:c.1005+151T=	NP_001350671.1:n.1005+151T=
XM_005246084.2:c.573+151T=	XP_005246141.1:n.573+151T=
XM_005246086.2:c.522+151T=	XP_005246143.1:n.522+151T=
XM_006712608.3:c.753+151T=	XP_006712671.1:n.753+151T=
XR_001738801.2:n.1135+151T=
XR_241242.3:n.1186+151T=
NM_030803.7:c.954+151T= MANE Select	NP_110430.5:n.954+151T=
NM_001190266.2:c.702+151T=	NP_001177195.1:n.702+151T=
NM_001190267.2:c.606+151T=	NP_001177196.1:n.606+151T=
NM_001363742.2:c.1005+151T=	NP_001350671.1:n.1005+151T=
NM_017974.4:c.897+151T=	NP_060444.3:n.897+151T=
NM_198890.3:c.465+151T=	NP_942593.2:n.465+151T=