Canonical Allele Identifier: CA351046229
Gene: ATG16L1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233274695T>C , CM000664.2:g.233274695T>C GRCh38
NC_000002.11:g.234183341T>C , CM000664.1:g.234183341T>C GRCh37
NC_000002.10:g.233848080T>C NCBI36
NG_023038.1:g.28125T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000392017.9:c.871T>C MANE Select ENSP00000375872.4:p.Phe291Leu
ENST00000347464.9:c.382T>C ENSP00000318259.6:p.Phe128Leu
ENST00000373525.9:c.439T>C ENSP00000362625.5:p.Phe147Leu
ENST00000392017.8:c.871T>C ENSP00000375872.4:p.Phe291Leu
ENST00000392018.1:c.922T>C ENSP00000375873.1:p.Phe308Leu
ENST00000392020.8:c.814T>C ENSP00000375875.4:p.Phe272Leu
ENST00000392021.7:c.*752T>C ENSP00000375876.3:n.*752T>C
ENST00000419681.5:c.382T>C ENSP00000398773.1:p.Phe128Leu
ENST00000444735.5:c.490T>C ENSP00000409215.1:p.Phe164Leu
ENST00000474148.5:n.1666T>C
ENST00000479942.5:n.1017T>C
ENST00000492298.5:n.392T>C
ENST00000498620.5:n.378T>C
NM_001190266.1:c.619T>C NP_001177195.1:p.Phe207Leu
NM_001190267.1:c.523T>C NP_001177196.1:p.Phe175Leu
NM_017974.3:c.814T>C NP_060444.3:p.Phe272Leu
NM_030803.6:c.871T>C NP_110430.5:p.Phe291Leu
NM_198890.2:c.382T>C NP_942593.2:p.Phe128Leu
XM_005246082.1:c.922T>C XP_005246139.1:p.Phe308Leu
XM_005246084.1:c.490T>C XP_005246141.1:p.Phe164Leu
XM_005246086.1:c.439T>C XP_005246143.1:p.Phe147Leu
XM_006712608.1:c.670T>C XP_006712671.1:p.Phe224Leu
XR_241242.1:n.1116T>C
NM_001363742.1:c.922T>C NP_001350671.1:p.Phe308Leu
XM_005246084.2:c.490T>C XP_005246141.1:p.Phe164Leu
XM_005246086.2:c.439T>C XP_005246143.1:p.Phe147Leu
XM_006712608.3:c.670T>C XP_006712671.1:p.Phe224Leu
XR_001738801.2:n.1052T>C
XR_241242.3:n.1103T>C
NM_030803.7:c.871T>C MANE Select NP_110430.5:p.Phe291Leu
NM_001190266.2:c.619T>C NP_001177195.1:p.Phe207Leu
NM_001190267.2:c.523T>C NP_001177196.1:p.Phe175Leu
NM_001363742.2:c.922T>C NP_001350671.1:p.Phe308Leu
NM_017974.4:c.814T>C NP_060444.3:p.Phe272Leu
NM_198890.3:c.382T>C NP_942593.2:p.Phe128Leu