Canonical Allele Identifier: CA435423823
Gene: ILDR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.121712494T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993647T>G , CM000665.2:g.121993647T>G GRCh38
NC_000003.11:g.121712494T>G , CM000665.1:g.121712494T>G GRCh37
NC_000003.10:g.123195184T>G NCBI36
NG_031870.1:g.33634A>C
NG_031870.2:g.71908A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1102A>C MANE Select ENSP00000345667.5:p.Arg368=
ENST00000460554.2:n.1052A>C
ENST00000642615.1:c.*285A>C ENSP00000495499.1:n.*285A>C
ENST00000273691.7:c.970A>C ENSP00000273691.3:p.Arg324=
ENST00000344209.9:c.1102A>C ENSP00000345667.5:p.Arg368=
ENST00000393631.5:c.835A>C ENSP00000377251.1:p.Arg279=
ENST00000460554.1:n.1204A>C
ENST00000462014.1:c.1006A>C ENSP00000419414.1:p.Arg336=
NM_001199799.1:c.1102A>C NP_001186728.1:p.Arg368=
NM_001199800.1:c.835A>C NP_001186729.1:p.Arg279=
NM_175924.3:c.970A>C NP_787120.1:p.Arg324=
XM_005247389.3:c.1006A>C XP_005247446.1:p.Arg336=
XM_011512738.1:c.1102A>C XP_011511040.1:p.Arg368=
XM_011512739.1:c.565A>C XP_011511041.1:p.Arg189=
XM_005247389.4:c.1006A>C XP_005247446.1:p.Arg336=
XM_011512738.2:c.1102A>C XP_011511040.1:p.Arg368=
XM_011512739.2:c.565A>C XP_011511041.1:p.Arg189=
NM_001199799.2:c.1102A>C MANE Select NP_001186728.1:p.Arg368=
NM_001199800.2:c.835A>C NP_001186729.1:p.Arg279=
NM_175924.4:c.970A>C NP_787120.1:p.Arg324=