Canonical Allele Identifier: CA435423835
Gene: ILDR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.121712503T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993656T>G , CM000665.2:g.121993656T>G GRCh38
NC_000003.11:g.121712503T>G , CM000665.1:g.121712503T>G GRCh37
NC_000003.10:g.123195193T>G NCBI36
NG_031870.1:g.33625A>C
NG_031870.2:g.71899A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1093A>C MANE Select ENSP00000345667.5:p.Arg365=
ENST00000460554.2:n.1043A>C
ENST00000642615.1:c.*276A>C ENSP00000495499.1:n.*276A>C
ENST00000273691.7:c.961A>C ENSP00000273691.3:p.Arg321=
ENST00000344209.9:c.1093A>C ENSP00000345667.5:p.Arg365=
ENST00000393631.5:c.826A>C ENSP00000377251.1:p.Arg276=
ENST00000460554.1:n.1195A>C
ENST00000462014.1:c.997A>C ENSP00000419414.1:p.Arg333=
NM_001199799.1:c.1093A>C NP_001186728.1:p.Arg365=
NM_001199800.1:c.826A>C NP_001186729.1:p.Arg276=
NM_175924.3:c.961A>C NP_787120.1:p.Arg321=
XM_005247389.3:c.997A>C XP_005247446.1:p.Arg333=
XM_011512738.1:c.1093A>C XP_011511040.1:p.Arg365=
XM_011512739.1:c.556A>C XP_011511041.1:p.Arg186=
XM_005247389.4:c.997A>C XP_005247446.1:p.Arg333=
XM_011512738.2:c.1093A>C XP_011511040.1:p.Arg365=
XM_011512739.2:c.556A>C XP_011511041.1:p.Arg186=
NM_001199799.2:c.1093A>C MANE Select NP_001186728.1:p.Arg365=
NM_001199800.2:c.826A>C NP_001186729.1:p.Arg276=
NM_175924.4:c.961A>C NP_787120.1:p.Arg321=