Canonical Allele Identifier: CA1397763149

Gene: ILDR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.122022079C= , CM000665.2:g.122022079C=	GRCh38
NC_000003.11:g.121740926C= , CM000665.1:g.121740926C=	GRCh37
NC_000003.10:g.123223616C=	NCBI36
NG_031870.1:g.5202G=
NG_031870.2:g.43476G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.-2G= MANE Select	ENSP00000345667.5:n.-2G=
ENST00000642615.1:c.-2G=	ENSP00000495499.1:n.-2G=
ENST00000273691.7:c.-2G=	ENSP00000273691.3:n.-2G=
ENST00000344209.9:c.-2G=	ENSP00000345667.5:n.-2G=
ENST00000393631.5:c.-2G=	ENSP00000377251.1:n.-2G=
ENST00000460554.1:n.120G=
NM_001199799.1:c.-2G=	NP_001186728.1:n.-2G=
NM_001199800.1:c.-2G=	NP_001186729.1:n.-2G=
NM_175924.3:c.-2G=	NP_787120.1:n.-2G=
XM_011512738.1:c.-2G=	XP_011511040.1:n.-2G=
XM_011512739.1:c.-347-14918G=	XP_011511041.1:n.-347-14918G=
XM_011512738.2:c.-2G=	XP_011511040.1:n.-2G=
XM_011512739.2:c.-347-14918G=	XP_011511041.1:n.-347-14918G=
NM_001199799.2:c.-2G= MANE Select	NP_001186728.1:n.-2G=
NM_001199800.2:c.-2G=	NP_001186729.1:n.-2G=
NM_175924.4:c.-2G=	NP_787120.1:n.-2G=