Canonical Allele Identifier: CA354143997
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993692A>C , CM000665.2:g.121993692A>C GRCh38
NC_000003.11:g.121712539A>C , CM000665.1:g.121712539A>C GRCh37
NC_000003.10:g.123195229A>C NCBI36
NG_031870.1:g.33589T>G
NG_031870.2:g.71863T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1057T>G MANE Select ENSP00000345667.5:p.Trp353Gly
ENST00000460554.2:n.1007T>G
ENST00000642615.1:c.*240T>G ENSP00000495499.1:n.*240T>G
ENST00000273691.7:c.925T>G ENSP00000273691.3:p.Trp309Gly
ENST00000344209.9:c.1057T>G ENSP00000345667.5:p.Trp353Gly
ENST00000393631.5:c.790T>G ENSP00000377251.1:p.Trp264Gly
ENST00000460554.1:n.1159T>G
ENST00000462014.1:c.961T>G ENSP00000419414.1:p.Trp321Gly
NM_001199799.1:c.1057T>G NP_001186728.1:p.Trp353Gly
NM_001199800.1:c.790T>G NP_001186729.1:p.Trp264Gly
NM_175924.3:c.925T>G NP_787120.1:p.Trp309Gly
XM_005247389.3:c.961T>G XP_005247446.1:p.Trp321Gly
XM_011512738.1:c.1057T>G XP_011511040.1:p.Trp353Gly
XM_011512739.1:c.520T>G XP_011511041.1:p.Trp174Gly
XM_005247389.4:c.961T>G XP_005247446.1:p.Trp321Gly
XM_011512738.2:c.1057T>G XP_011511040.1:p.Trp353Gly
XM_011512739.2:c.520T>G XP_011511041.1:p.Trp174Gly
NM_001199799.2:c.1057T>G MANE Select NP_001186728.1:p.Trp353Gly
NM_001199800.2:c.790T>G NP_001186729.1:p.Trp264Gly
NM_175924.4:c.925T>G NP_787120.1:p.Trp309Gly