Canonical Allele Identifier: CA1397750899

Gene: ILDR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993584C= , CM000665.2:g.121993584C=	GRCh38
NC_000003.11:g.121712431C= , CM000665.1:g.121712431C=	GRCh37
NC_000003.10:g.123195121C=	NCBI36
NG_031870.1:g.33697G=
NG_031870.2:g.71971G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1165G= MANE Select	ENSP00000345667.5:p.Ala389=
ENST00000460554.2:n.1115G=
ENST00000642615.1:c.*348G=	ENSP00000495499.1:n.*348G=
ENST00000273691.7:c.1033G=	ENSP00000273691.3:p.Ala345=
ENST00000344209.9:c.1165G=	ENSP00000345667.5:p.Ala389=
ENST00000393631.5:c.898G=	ENSP00000377251.1:p.Ala300=
ENST00000460554.1:n.1267G=
ENST00000462014.1:c.1069G=	ENSP00000419414.1:p.Ala357=
NM_001199799.1:c.1165G=	NP_001186728.1:p.Ala389=
NM_001199800.1:c.898G=	NP_001186729.1:p.Ala300=
NM_175924.3:c.1033G=	NP_787120.1:p.Ala345=
XM_005247389.3:c.1069G=	XP_005247446.1:p.Ala357=
XM_011512738.1:c.1165G=	XP_011511040.1:p.Ala389=
XM_011512739.1:c.628G=	XP_011511041.1:p.Ala210=
XM_005247389.4:c.1069G=	XP_005247446.1:p.Ala357=
XM_011512738.2:c.1165G=	XP_011511040.1:p.Ala389=
XM_011512739.2:c.628G=	XP_011511041.1:p.Ala210=
NM_001199799.2:c.1165G= MANE Select	NP_001186728.1:p.Ala389=
NM_001199800.2:c.898G=	NP_001186729.1:p.Ala300=
NM_175924.4:c.1033G=	NP_787120.1:p.Ala345=