Canonical Allele Identifier: CA2754678580

Gene: ATG16L1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233275637T>G , CM000664.2:g.233275637T>G	GRCh38
NC_000002.11:g.234184283T>G , CM000664.1:g.234184283T>G	GRCh37
NC_000002.10:g.233849022T>G	NCBI36
NG_023038.1:g.29067T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392017.9:c.954+859T>G MANE Select	ENSP00000375872.4:n.954+859T>G
ENST00000347464.9:c.465+859T>G	ENSP00000318259.6:n.465+859T>G
ENST00000373525.9:c.522+859T>G	ENSP00000362625.5:n.522+859T>G
ENST00000392017.8:c.954+859T>G	ENSP00000375872.4:n.954+859T>G
ENST00000392018.1:c.1005+859T>G	ENSP00000375873.1:n.1005+859T>G
ENST00000392020.8:c.897+859T>G	ENSP00000375875.4:n.897+859T>G
ENST00000392021.7:c.*835+859T>G	ENSP00000375876.3:n.*835+859T>G
ENST00000419681.5:c.465+859T>G	ENSP00000398773.1:n.465+859T>G
ENST00000464645.5:n.89+170T>G
ENST00000474148.5:n.1749+859T>G
ENST00000479942.5:n.1100+859T>G
ENST00000492298.5:n.475+859T>G
ENST00000498620.5:n.461+859T>G
NM_001190266.1:c.702+859T>G	NP_001177195.1:n.702+859T>G
NM_001190267.1:c.606+859T>G	NP_001177196.1:n.606+859T>G
NM_017974.3:c.897+859T>G	NP_060444.3:n.897+859T>G
NM_030803.6:c.954+859T>G	NP_110430.5:n.954+859T>G
NM_198890.2:c.465+859T>G	NP_942593.2:n.465+859T>G
XM_005246082.1:c.1005+859T>G	XP_005246139.1:n.1005+859T>G
XM_005246084.1:c.573+859T>G	XP_005246141.1:n.573+859T>G
XM_005246086.1:c.522+859T>G	XP_005246143.1:n.522+859T>G
XM_006712608.1:c.753+859T>G	XP_006712671.1:n.753+859T>G
XR_241242.1:n.1199+859T>G
NM_001363742.1:c.1005+859T>G	NP_001350671.1:n.1005+859T>G
XM_005246084.2:c.573+859T>G	XP_005246141.1:n.573+859T>G
XM_005246086.2:c.522+859T>G	XP_005246143.1:n.522+859T>G
XM_006712608.3:c.753+859T>G	XP_006712671.1:n.753+859T>G
XR_001738801.2:n.1135+859T>G
XR_241242.3:n.1186+859T>G
NM_030803.7:c.954+859T>G MANE Select	NP_110430.5:n.954+859T>G
NM_001190266.2:c.702+859T>G	NP_001177195.1:n.702+859T>G
NM_001190267.2:c.606+859T>G	NP_001177196.1:n.606+859T>G
NM_001363742.2:c.1005+859T>G	NP_001350671.1:n.1005+859T>G
NM_017974.4:c.897+859T>G	NP_060444.3:n.897+859T>G
NM_198890.3:c.465+859T>G	NP_942593.2:n.465+859T>G