Canonical Allele Identifier: CA354141754

Gene: ILDR1

Linked Data

• dbSNP Id: rs1384960809
• MyVariant Identifiers: chr3:g.121712007T>G (hg19) ; chr3:g.121993160T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993160T>G , CM000665.2:g.121993160T>G	GRCh38
NC_000003.11:g.121712007T>G , CM000665.1:g.121712007T>G	GRCh37
NC_000003.10:g.123194697T>G	NCBI36
NG_031870.1:g.34121A>C
NG_031870.2:g.72395A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1589A>C MANE Select	ENSP00000345667.5:p.Glu530Ala
ENST00000460554.2:n.1539A>C
ENST00000642615.1:c.*772A>C	ENSP00000495499.1:n.*772A>C
ENST00000273691.7:c.1457A>C	ENSP00000273691.3:p.Glu486Ala
ENST00000344209.9:c.1589A>C	ENSP00000345667.5:p.Glu530Ala
ENST00000393631.5:c.1322A>C	ENSP00000377251.1:p.Glu441Ala
ENST00000460554.1:n.1691A>C
ENST00000462014.1:c.1493A>C	ENSP00000419414.1:p.Glu498Ala
NM_001199799.1:c.1589A>C	NP_001186728.1:p.Glu530Ala
NM_001199800.1:c.1322A>C	NP_001186729.1:p.Glu441Ala
NM_175924.3:c.1457A>C	NP_787120.1:p.Glu486Ala
XM_005247389.3:c.1493A>C	XP_005247446.1:p.Glu498Ala
XM_011512738.1:c.1558+31A>C	XP_011511040.1:n.1558+31A>C
XM_011512739.1:c.1052A>C	XP_011511041.1:p.Glu351Ala
XM_005247389.4:c.1493A>C	XP_005247446.1:p.Glu498Ala
XM_011512738.2:c.1558+31A>C	XP_011511040.1:n.1558+31A>C
XM_011512739.2:c.1052A>C	XP_011511041.1:p.Glu351Ala
NM_001199799.2:c.1589A>C MANE Select	NP_001186728.1:p.Glu530Ala
NM_001199800.2:c.1322A>C	NP_001186729.1:p.Glu441Ala
NM_175924.4:c.1457A>C	NP_787120.1:p.Glu486Ala