Canonical Allele Identifier: CA1397750904

Gene: ILDR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993590A= , CM000665.2:g.121993590A=	GRCh38
NC_000003.11:g.121712437A= , CM000665.1:g.121712437A=	GRCh37
NC_000003.10:g.123195127A=	NCBI36
NG_031870.1:g.33691T=
NG_031870.2:g.71965T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1159T= MANE Select	ENSP00000345667.5:p.Ser387=
ENST00000460554.2:n.1109T=
ENST00000642615.1:c.*342T=	ENSP00000495499.1:n.*342T=
ENST00000273691.7:c.1027T=	ENSP00000273691.3:p.Ser343=
ENST00000344209.9:c.1159T=	ENSP00000345667.5:p.Ser387=
ENST00000393631.5:c.892T=	ENSP00000377251.1:p.Ser298=
ENST00000460554.1:n.1261T=
ENST00000462014.1:c.1063T=	ENSP00000419414.1:p.Ser355=
NM_001199799.1:c.1159T=	NP_001186728.1:p.Ser387=
NM_001199800.1:c.892T=	NP_001186729.1:p.Ser298=
NM_175924.3:c.1027T=	NP_787120.1:p.Ser343=
XM_005247389.3:c.1063T=	XP_005247446.1:p.Ser355=
XM_011512738.1:c.1159T=	XP_011511040.1:p.Ser387=
XM_011512739.1:c.622T=	XP_011511041.1:p.Ser208=
XM_005247389.4:c.1063T=	XP_005247446.1:p.Ser355=
XM_011512738.2:c.1159T=	XP_011511040.1:p.Ser387=
XM_011512739.2:c.622T=	XP_011511041.1:p.Ser208=
NM_001199799.2:c.1159T= MANE Select	NP_001186728.1:p.Ser387=
NM_001199800.2:c.892T=	NP_001186729.1:p.Ser298=
NM_175924.4:c.1027T=	NP_787120.1:p.Ser343=