Canonical Allele Identifier: CA435423831

Gene: ILDR1

Linked Data

• COSMIC: COSM1719152 ; COSM1719153 ; COSM3586145
• MyVariant Identifiers: chr3:g.121712501C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.121993654C>T , CM000665.2:g.121993654C>T	GRCh38
NC_000003.11:g.121712501C>T , CM000665.1:g.121712501C>T	GRCh37
NC_000003.10:g.123195191C>T	NCBI36
NG_031870.1:g.33627G>A
NG_031870.2:g.71901G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344209.10:c.1095G>A MANE Select	ENSP00000345667.5:p.Arg365=
ENST00000460554.2:n.1045G>A
ENST00000642615.1:c.*278G>A	ENSP00000495499.1:n.*278G>A
ENST00000273691.7:c.963G>A	ENSP00000273691.3:p.Arg321=
ENST00000344209.9:c.1095G>A	ENSP00000345667.5:p.Arg365=
ENST00000393631.5:c.828G>A	ENSP00000377251.1:p.Arg276=
ENST00000460554.1:n.1197G>A
ENST00000462014.1:c.999G>A	ENSP00000419414.1:p.Arg333=
NM_001199799.1:c.1095G>A	NP_001186728.1:p.Arg365=
NM_001199800.1:c.828G>A	NP_001186729.1:p.Arg276=
NM_175924.3:c.963G>A	NP_787120.1:p.Arg321=
XM_005247389.3:c.999G>A	XP_005247446.1:p.Arg333=
XM_011512738.1:c.1095G>A	XP_011511040.1:p.Arg365=
XM_011512739.1:c.558G>A	XP_011511041.1:p.Arg186=
XM_005247389.4:c.999G>A	XP_005247446.1:p.Arg333=
XM_011512738.2:c.1095G>A	XP_011511040.1:p.Arg365=
XM_011512739.2:c.558G>A	XP_011511041.1:p.Arg186=
NM_001199799.2:c.1095G>A MANE Select	NP_001186728.1:p.Arg365=
NM_001199800.2:c.828G>A	NP_001186729.1:p.Arg276=
NM_175924.4:c.963G>A	NP_787120.1:p.Arg321=