Canonical Allele Identifier: CA1335666672
Gene: ATG16L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233274722A= , CM000664.2:g.233274722A= GRCh38
NC_000002.11:g.234183368A= , CM000664.1:g.234183368A= GRCh37
NC_000002.10:g.233848107A= NCBI36
NG_023038.1:g.28152A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000392017.9:c.898A= MANE Select ENSP00000375872.4:p.Thr300=
ENST00000347464.9:c.409A= ENSP00000318259.6:p.Thr137=
ENST00000373525.9:c.466A= ENSP00000362625.5:p.Thr156=
ENST00000392017.8:c.898A= ENSP00000375872.4:p.Thr300=
ENST00000392018.1:c.949A= ENSP00000375873.1:p.Thr317=
ENST00000392020.8:c.841A= ENSP00000375875.4:p.Thr281=
ENST00000392021.7:c.*779A= ENSP00000375876.3:n.*779A=
ENST00000419681.5:c.409A= ENSP00000398773.1:p.Thr137=
ENST00000444735.5:c.517A= ENSP00000409215.1:p.Thr173=
ENST00000474148.5:n.1693A=
ENST00000479942.5:n.1044A=
ENST00000492298.5:n.419A=
ENST00000498620.5:n.405A=
NM_001190266.1:c.646A= NP_001177195.1:p.Thr216=
NM_001190267.1:c.550A= NP_001177196.1:p.Thr184=
NM_017974.3:c.841A= NP_060444.3:p.Thr281=
NM_030803.6:c.898A= NP_110430.5:p.Thr300=
NM_198890.2:c.409A= NP_942593.2:p.Thr137=
XM_005246082.1:c.949A= XP_005246139.1:p.Thr317=
XM_005246084.1:c.517A= XP_005246141.1:p.Thr173=
XM_005246086.1:c.466A= XP_005246143.1:p.Thr156=
XM_006712608.1:c.697A= XP_006712671.1:p.Thr233=
XR_241242.1:n.1143A=
NM_001363742.1:c.949A= NP_001350671.1:p.Thr317=
XM_005246084.2:c.517A= XP_005246141.1:p.Thr173=
XM_005246086.2:c.466A= XP_005246143.1:p.Thr156=
XM_006712608.3:c.697A= XP_006712671.1:p.Thr233=
XR_001738801.2:n.1079A=
XR_241242.3:n.1130A=
NM_030803.7:c.898A= MANE Select NP_110430.5:p.Thr300=
NM_001190266.2:c.646A= NP_001177195.1:p.Thr216=
NM_001190267.2:c.550A= NP_001177196.1:p.Thr184=
NM_001363742.2:c.949A= NP_001350671.1:p.Thr317=
NM_017974.4:c.841A= NP_060444.3:p.Thr281=
NM_198890.3:c.409A= NP_942593.2:p.Thr137=