Canonical Allele Identifier: CA1397750888

Gene: ILDR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993560G= , CM000665.2:g.121993560G=	GRCh38
NC_000003.11:g.121712407G= , CM000665.1:g.121712407G=	GRCh37
NC_000003.10:g.123195097G=	NCBI36
NG_031870.1:g.33721C=
NG_031870.2:g.71995C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1189C= MANE Select	ENSP00000345667.5:p.Pro397=
ENST00000460554.2:n.1139C=
ENST00000642615.1:c.*372C=	ENSP00000495499.1:n.*372C=
ENST00000273691.7:c.1057C=	ENSP00000273691.3:p.Pro353=
ENST00000344209.9:c.1189C=	ENSP00000345667.5:p.Pro397=
ENST00000393631.5:c.922C=	ENSP00000377251.1:p.Pro308=
ENST00000460554.1:n.1291C=
ENST00000462014.1:c.1093C=	ENSP00000419414.1:p.Pro365=
NM_001199799.1:c.1189C=	NP_001186728.1:p.Pro397=
NM_001199800.1:c.922C=	NP_001186729.1:p.Pro308=
NM_175924.3:c.1057C=	NP_787120.1:p.Pro353=
XM_005247389.3:c.1093C=	XP_005247446.1:p.Pro365=
XM_011512738.1:c.1189C=	XP_011511040.1:p.Pro397=
XM_011512739.1:c.652C=	XP_011511041.1:p.Pro218=
XM_005247389.4:c.1093C=	XP_005247446.1:p.Pro365=
XM_011512738.2:c.1189C=	XP_011511040.1:p.Pro397=
XM_011512739.2:c.652C=	XP_011511041.1:p.Pro218=
NM_001199799.2:c.1189C= MANE Select	NP_001186728.1:p.Pro397=
NM_001199800.2:c.922C=	NP_001186729.1:p.Pro308=
NM_175924.4:c.1057C=	NP_787120.1:p.Pro353=