Canonical Allele Identifier: CA435423768
Gene: ILDR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.121712453C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993606C>T , CM000665.2:g.121993606C>T GRCh38
NC_000003.11:g.121712453C>T , CM000665.1:g.121712453C>T GRCh37
NC_000003.10:g.123195143C>T NCBI36
NG_031870.1:g.33675G>A
NG_031870.2:g.71949G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1143G>A MANE Select ENSP00000345667.5:p.Gln381=
ENST00000460554.2:n.1093G>A
ENST00000642615.1:c.*326G>A ENSP00000495499.1:n.*326G>A
ENST00000273691.7:c.1011G>A ENSP00000273691.3:p.Gln337=
ENST00000344209.9:c.1143G>A ENSP00000345667.5:p.Gln381=
ENST00000393631.5:c.876G>A ENSP00000377251.1:p.Gln292=
ENST00000460554.1:n.1245G>A
ENST00000462014.1:c.1047G>A ENSP00000419414.1:p.Gln349=
NM_001199799.1:c.1143G>A NP_001186728.1:p.Gln381=
NM_001199800.1:c.876G>A NP_001186729.1:p.Gln292=
NM_175924.3:c.1011G>A NP_787120.1:p.Gln337=
XM_005247389.3:c.1047G>A XP_005247446.1:p.Gln349=
XM_011512738.1:c.1143G>A XP_011511040.1:p.Gln381=
XM_011512739.1:c.606G>A XP_011511041.1:p.Gln202=
XM_005247389.4:c.1047G>A XP_005247446.1:p.Gln349=
XM_011512738.2:c.1143G>A XP_011511040.1:p.Gln381=
XM_011512739.2:c.606G>A XP_011511041.1:p.Gln202=
NM_001199799.2:c.1143G>A MANE Select NP_001186728.1:p.Gln381=
NM_001199800.2:c.876G>A NP_001186729.1:p.Gln292=
NM_175924.4:c.1011G>A NP_787120.1:p.Gln337=