Canonical Allele Identifier: CA1397750709

Gene: ILDR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993219A= , CM000665.2:g.121993219A=	GRCh38
NC_000003.11:g.121712066A= , CM000665.1:g.121712066A=	GRCh37
NC_000003.10:g.123194756A=	NCBI36
NG_031870.1:g.34062T=
NG_031870.2:g.72336T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1530T= MANE Select	ENSP00000345667.5:p.Pro510=
ENST00000460554.2:n.1480T=
ENST00000642615.1:c.*713T=	ENSP00000495499.1:n.*713T=
ENST00000273691.7:c.1398T=	ENSP00000273691.3:p.Pro466=
ENST00000344209.9:c.1530T=	ENSP00000345667.5:p.Pro510=
ENST00000393631.5:c.1263T=	ENSP00000377251.1:p.Pro421=
ENST00000460554.1:n.1632T=
ENST00000462014.1:c.1434T=	ENSP00000419414.1:p.Pro478=
NM_001199799.1:c.1530T=	NP_001186728.1:p.Pro510=
NM_001199800.1:c.1263T=	NP_001186729.1:p.Pro421=
NM_175924.3:c.1398T=	NP_787120.1:p.Pro466=
XM_005247389.3:c.1434T=	XP_005247446.1:p.Pro478=
XM_011512738.1:c.1530T=	XP_011511040.1:p.Pro510=
XM_011512739.1:c.993T=	XP_011511041.1:p.Pro331=
XM_005247389.4:c.1434T=	XP_005247446.1:p.Pro478=
XM_011512738.2:c.1530T=	XP_011511040.1:p.Pro510=
XM_011512739.2:c.993T=	XP_011511041.1:p.Pro331=
NM_001199799.2:c.1530T= MANE Select	NP_001186728.1:p.Pro510=
NM_001199800.2:c.1263T=	NP_001186729.1:p.Pro421=
NM_175924.4:c.1398T=	NP_787120.1:p.Pro466=