Canonical Allele Identifier: CA354144002
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993694T>C , CM000665.2:g.121993694T>C GRCh38
NC_000003.11:g.121712541T>C , CM000665.1:g.121712541T>C GRCh37
NC_000003.10:g.123195231T>C NCBI36
NG_031870.1:g.33587A>G
NG_031870.2:g.71861A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1055A>G MANE Select ENSP00000345667.5:p.Gln352Arg
ENST00000460554.2:n.1005A>G
ENST00000642615.1:c.*238A>G ENSP00000495499.1:n.*238A>G
ENST00000273691.7:c.923A>G ENSP00000273691.3:p.Gln308Arg
ENST00000344209.9:c.1055A>G ENSP00000345667.5:p.Gln352Arg
ENST00000393631.5:c.788A>G ENSP00000377251.1:p.Gln263Arg
ENST00000460554.1:n.1157A>G
ENST00000462014.1:c.959A>G ENSP00000419414.1:p.Gln320Arg
NM_001199799.1:c.1055A>G NP_001186728.1:p.Gln352Arg
NM_001199800.1:c.788A>G NP_001186729.1:p.Gln263Arg
NM_175924.3:c.923A>G NP_787120.1:p.Gln308Arg
XM_005247389.3:c.959A>G XP_005247446.1:p.Gln320Arg
XM_011512738.1:c.1055A>G XP_011511040.1:p.Gln352Arg
XM_011512739.1:c.518A>G XP_011511041.1:p.Gln173Arg
XM_005247389.4:c.959A>G XP_005247446.1:p.Gln320Arg
XM_011512738.2:c.1055A>G XP_011511040.1:p.Gln352Arg
XM_011512739.2:c.518A>G XP_011511041.1:p.Gln173Arg
NM_001199799.2:c.1055A>G MANE Select NP_001186728.1:p.Gln352Arg
NM_001199800.2:c.788A>G NP_001186729.1:p.Gln263Arg
NM_175924.4:c.923A>G NP_787120.1:p.Gln308Arg