Canonical Allele Identifier: CA1397763174

Gene: ILDR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122022121A= , CM000665.2:g.122022121A=	GRCh38
NC_000003.11:g.121740968A= , CM000665.1:g.121740968A=	GRCh37
NC_000003.10:g.123223658A=	NCBI36
NG_031870.1:g.5160T=
NG_031870.2:g.43434T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.-44T= MANE Select	ENSP00000345667.5:n.-44T=
ENST00000642615.1:c.-44T=	ENSP00000495499.1:n.-44T=
ENST00000273691.7:c.-44T=	ENSP00000273691.3:n.-44T=
ENST00000344209.9:c.-44T=	ENSP00000345667.5:n.-44T=
ENST00000393631.5:c.-44T=	ENSP00000377251.1:n.-44T=
ENST00000460554.1:n.78T=
NM_001199799.1:c.-44T=	NP_001186728.1:n.-44T=
NM_001199800.1:c.-44T=	NP_001186729.1:n.-44T=
NM_175924.3:c.-44T=	NP_787120.1:n.-44T=
XM_011512738.1:c.-44T=	XP_011511040.1:n.-44T=
XM_011512739.1:c.-347-14960T=	XP_011511041.1:n.-347-14960T=
XM_011512738.2:c.-44T=	XP_011511040.1:n.-44T=
XM_011512739.2:c.-347-14960T=	XP_011511041.1:n.-347-14960T=
NM_001199799.2:c.-44T= MANE Select	NP_001186728.1:n.-44T=
NM_001199800.2:c.-44T=	NP_001186729.1:n.-44T=
NM_175924.4:c.-44T=	NP_787120.1:n.-44T=