Canonical Allele Identifier: CA354143064
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1297C>G MANE Select ENSP00000345667.5:p.Arg433Gly
ENST00000460554.2:n.1247C>G
ENST00000642615.1:c.*480C>G ENSP00000495499.1:n.*480C>G
ENST00000273691.7:c.1165C>G ENSP00000273691.3:p.Arg389Gly
ENST00000344209.9:c.1297C>G ENSP00000345667.5:p.Arg433Gly
ENST00000393631.5:c.1030C>G ENSP00000377251.1:p.Arg344Gly
ENST00000460554.1:n.1399C>G
ENST00000462014.1:c.1201C>G ENSP00000419414.1:p.Arg401Gly
NM_001199799.1:c.1297C>G NP_001186728.1:p.Arg433Gly
NM_001199800.1:c.1030C>G NP_001186729.1:p.Arg344Gly
NM_175924.3:c.1165C>G NP_787120.1:p.Arg389Gly
XM_005247389.3:c.1201C>G XP_005247446.1:p.Arg401Gly
XM_011512738.1:c.1297C>G XP_011511040.1:p.Arg433Gly
XM_011512739.1:c.760C>G XP_011511041.1:p.Arg254Gly
XM_005247389.4:c.1201C>G XP_005247446.1:p.Arg401Gly
XM_011512738.2:c.1297C>G XP_011511040.1:p.Arg433Gly
XM_011512739.2:c.760C>G XP_011511041.1:p.Arg254Gly
NM_001199799.2:c.1297C>G MANE Select NP_001186728.1:p.Arg433Gly
NM_001199800.2:c.1030C>G NP_001186729.1:p.Arg344Gly
NM_175924.4:c.1165C>G NP_787120.1:p.Arg389Gly