Canonical Allele Identifier: CA431820798

Gene: ATG16L1

Linked Data

• MyVariant Identifiers: chr2:g.234183331T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233274685T>A , CM000664.2:g.233274685T>A	GRCh38
NC_000002.11:g.234183331T>A , CM000664.1:g.234183331T>A	GRCh37
NC_000002.10:g.233848070T>A	NCBI36
NG_023038.1:g.28115T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392017.9:c.861T>A MANE Select	ENSP00000375872.4:p.Ser287=
ENST00000347464.9:c.372T>A	ENSP00000318259.6:p.Ser124=
ENST00000373525.9:c.429T>A	ENSP00000362625.5:p.Ser143=
ENST00000392017.8:c.861T>A	ENSP00000375872.4:p.Ser287=
ENST00000392018.1:c.912T>A	ENSP00000375873.1:p.Ser304=
ENST00000392020.8:c.804T>A	ENSP00000375875.4:p.Ser268=
ENST00000392021.7:c.*742T>A	ENSP00000375876.3:n.*742T>A
ENST00000419681.5:c.372T>A	ENSP00000398773.1:p.Ser124=
ENST00000444735.5:c.480T>A	ENSP00000409215.1:p.Ser160=
ENST00000474148.5:n.1656T>A
ENST00000479942.5:n.1007T>A
ENST00000492298.5:n.382T>A
ENST00000498620.5:n.368T>A
NM_001190266.1:c.609T>A	NP_001177195.1:p.Ser203=
NM_001190267.1:c.513T>A	NP_001177196.1:p.Ser171=
NM_017974.3:c.804T>A	NP_060444.3:p.Ser268=
NM_030803.6:c.861T>A	NP_110430.5:p.Ser287=
NM_198890.2:c.372T>A	NP_942593.2:p.Ser124=
XM_005246082.1:c.912T>A	XP_005246139.1:p.Ser304=
XM_005246084.1:c.480T>A	XP_005246141.1:p.Ser160=
XM_005246086.1:c.429T>A	XP_005246143.1:p.Ser143=
XM_006712608.1:c.660T>A	XP_006712671.1:p.Ser220=
XR_241242.1:n.1106T>A
NM_001363742.1:c.912T>A	NP_001350671.1:p.Ser304=
XM_005246084.2:c.480T>A	XP_005246141.1:p.Ser160=
XM_005246086.2:c.429T>A	XP_005246143.1:p.Ser143=
XM_006712608.3:c.660T>A	XP_006712671.1:p.Ser220=
XR_001738801.2:n.1042T>A
XR_241242.3:n.1093T>A
NM_030803.7:c.861T>A MANE Select	NP_110430.5:p.Ser287=
NM_001190266.2:c.609T>A	NP_001177195.1:p.Ser203=
NM_001190267.2:c.513T>A	NP_001177196.1:p.Ser171=
NM_001363742.2:c.912T>A	NP_001350671.1:p.Ser304=
NM_017974.4:c.804T>A	NP_060444.3:p.Ser268=
NM_198890.3:c.372T>A	NP_942593.2:p.Ser124=