Canonical Allele Identifier: CA1397750935

Gene: ILDR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993656T= , CM000665.2:g.121993656T=	GRCh38
NC_000003.11:g.121712503T= , CM000665.1:g.121712503T=	GRCh37
NC_000003.10:g.123195193T=	NCBI36
NG_031870.1:g.33625A=
NG_031870.2:g.71899A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1093A= MANE Select	ENSP00000345667.5:p.Arg365=
ENST00000460554.2:n.1043A=
ENST00000642615.1:c.*276A=	ENSP00000495499.1:n.*276A=
ENST00000273691.7:c.961A=	ENSP00000273691.3:p.Arg321=
ENST00000344209.9:c.1093A=	ENSP00000345667.5:p.Arg365=
ENST00000393631.5:c.826A=	ENSP00000377251.1:p.Arg276=
ENST00000460554.1:n.1195A=
ENST00000462014.1:c.997A=	ENSP00000419414.1:p.Arg333=
NM_001199799.1:c.1093A=	NP_001186728.1:p.Arg365=
NM_001199800.1:c.826A=	NP_001186729.1:p.Arg276=
NM_175924.3:c.961A=	NP_787120.1:p.Arg321=
XM_005247389.3:c.997A=	XP_005247446.1:p.Arg333=
XM_011512738.1:c.1093A=	XP_011511040.1:p.Arg365=
XM_011512739.1:c.556A=	XP_011511041.1:p.Arg186=
XM_005247389.4:c.997A=	XP_005247446.1:p.Arg333=
XM_011512738.2:c.1093A=	XP_011511040.1:p.Arg365=
XM_011512739.2:c.556A=	XP_011511041.1:p.Arg186=
NM_001199799.2:c.1093A= MANE Select	NP_001186728.1:p.Arg365=
NM_001199800.2:c.826A=	NP_001186729.1:p.Arg276=
NM_175924.4:c.961A=	NP_787120.1:p.Arg321=