Canonical Allele Identifier: CA435423933
Gene: ILDR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.121712566T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993719T>G , CM000665.2:g.121993719T>G GRCh38
NC_000003.11:g.121712566T>G , CM000665.1:g.121712566T>G GRCh37
NC_000003.10:g.123195256T>G NCBI36
NG_031870.1:g.33562A>C
NG_031870.2:g.71836A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1030A>C MANE Select ENSP00000345667.5:p.Arg344=
ENST00000460554.2:n.980A>C
ENST00000642615.1:c.*213A>C ENSP00000495499.1:n.*213A>C
ENST00000273691.7:c.898A>C ENSP00000273691.3:p.Arg300=
ENST00000344209.9:c.1030A>C ENSP00000345667.5:p.Arg344=
ENST00000393631.5:c.763A>C ENSP00000377251.1:p.Arg255=
ENST00000460554.1:n.1132A>C
ENST00000462014.1:c.934A>C ENSP00000419414.1:p.Arg312=
NM_001199799.1:c.1030A>C NP_001186728.1:p.Arg344=
NM_001199800.1:c.763A>C NP_001186729.1:p.Arg255=
NM_175924.3:c.898A>C NP_787120.1:p.Arg300=
XM_005247389.3:c.934A>C XP_005247446.1:p.Arg312=
XM_011512738.1:c.1030A>C XP_011511040.1:p.Arg344=
XM_011512739.1:c.493A>C XP_011511041.1:p.Arg165=
XM_005247389.4:c.934A>C XP_005247446.1:p.Arg312=
XM_011512738.2:c.1030A>C XP_011511040.1:p.Arg344=
XM_011512739.2:c.493A>C XP_011511041.1:p.Arg165=
NM_001199799.2:c.1030A>C MANE Select NP_001186728.1:p.Arg344=
NM_001199800.2:c.763A>C NP_001186729.1:p.Arg255=
NM_175924.4:c.898A>C NP_787120.1:p.Arg300=