Canonical Allele Identifier: CA435423672
Gene: ILDR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.121712299G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993452G>T , CM000665.2:g.121993452G>T GRCh38
NC_000003.11:g.121712299G>T , CM000665.1:g.121712299G>T GRCh37
NC_000003.10:g.123194989G>T NCBI36
NG_031870.1:g.33829C>A
NG_031870.2:g.72103C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1297C>A MANE Select ENSP00000345667.5:p.Arg433=
ENST00000460554.2:n.1247C>A
ENST00000642615.1:c.*480C>A ENSP00000495499.1:n.*480C>A
ENST00000273691.7:c.1165C>A ENSP00000273691.3:p.Arg389=
ENST00000344209.9:c.1297C>A ENSP00000345667.5:p.Arg433=
ENST00000393631.5:c.1030C>A ENSP00000377251.1:p.Arg344=
ENST00000460554.1:n.1399C>A
ENST00000462014.1:c.1201C>A ENSP00000419414.1:p.Arg401=
NM_001199799.1:c.1297C>A NP_001186728.1:p.Arg433=
NM_001199800.1:c.1030C>A NP_001186729.1:p.Arg344=
NM_175924.3:c.1165C>A NP_787120.1:p.Arg389=
XM_005247389.3:c.1201C>A XP_005247446.1:p.Arg401=
XM_011512738.1:c.1297C>A XP_011511040.1:p.Arg433=
XM_011512739.1:c.760C>A XP_011511041.1:p.Arg254=
XM_005247389.4:c.1201C>A XP_005247446.1:p.Arg401=
XM_011512738.2:c.1297C>A XP_011511040.1:p.Arg433=
XM_011512739.2:c.760C>A XP_011511041.1:p.Arg254=
NM_001199799.2:c.1297C>A MANE Select NP_001186728.1:p.Arg433=
NM_001199800.2:c.1030C>A NP_001186729.1:p.Arg344=
NM_175924.4:c.1165C>A NP_787120.1:p.Arg389=