Canonical Allele Identifier: CA1397750928

Gene: ILDR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993641G= , CM000665.2:g.121993641G=	GRCh38
NC_000003.11:g.121712488G= , CM000665.1:g.121712488G=	GRCh37
NC_000003.10:g.123195178G=	NCBI36
NG_031870.1:g.33640C=
NG_031870.2:g.71914C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1108C= MANE Select	ENSP00000345667.5:p.His370=
ENST00000460554.2:n.1058C=
ENST00000642615.1:c.*291C=	ENSP00000495499.1:n.*291C=
ENST00000273691.7:c.976C=	ENSP00000273691.3:p.His326=
ENST00000344209.9:c.1108C=	ENSP00000345667.5:p.His370=
ENST00000393631.5:c.841C=	ENSP00000377251.1:p.His281=
ENST00000460554.1:n.1210C=
ENST00000462014.1:c.1012C=	ENSP00000419414.1:p.His338=
NM_001199799.1:c.1108C=	NP_001186728.1:p.His370=
NM_001199800.1:c.841C=	NP_001186729.1:p.His281=
NM_175924.3:c.976C=	NP_787120.1:p.His326=
XM_005247389.3:c.1012C=	XP_005247446.1:p.His338=
XM_011512738.1:c.1108C=	XP_011511040.1:p.His370=
XM_011512739.1:c.571C=	XP_011511041.1:p.His191=
XM_005247389.4:c.1012C=	XP_005247446.1:p.His338=
XM_011512738.2:c.1108C=	XP_011511040.1:p.His370=
XM_011512739.2:c.571C=	XP_011511041.1:p.His191=
NM_001199799.2:c.1108C= MANE Select	NP_001186728.1:p.His370=
NM_001199800.2:c.841C=	NP_001186729.1:p.His281=
NM_175924.4:c.976C=	NP_787120.1:p.His326=