Canonical Allele Identifier: CA354144017
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993700T>C , CM000665.2:g.121993700T>C GRCh38
NC_000003.11:g.121712547T>C , CM000665.1:g.121712547T>C GRCh37
NC_000003.10:g.123195237T>C NCBI36
NG_031870.1:g.33581A>G
NG_031870.2:g.71855A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1049A>G MANE Select ENSP00000345667.5:p.His350Arg
ENST00000460554.2:n.999A>G
ENST00000642615.1:c.*232A>G ENSP00000495499.1:n.*232A>G
ENST00000273691.7:c.917A>G ENSP00000273691.3:p.His306Arg
ENST00000344209.9:c.1049A>G ENSP00000345667.5:p.His350Arg
ENST00000393631.5:c.782A>G ENSP00000377251.1:p.His261Arg
ENST00000460554.1:n.1151A>G
ENST00000462014.1:c.953A>G ENSP00000419414.1:p.His318Arg
NM_001199799.1:c.1049A>G NP_001186728.1:p.His350Arg
NM_001199800.1:c.782A>G NP_001186729.1:p.His261Arg
NM_175924.3:c.917A>G NP_787120.1:p.His306Arg
XM_005247389.3:c.953A>G XP_005247446.1:p.His318Arg
XM_011512738.1:c.1049A>G XP_011511040.1:p.His350Arg
XM_011512739.1:c.512A>G XP_011511041.1:p.His171Arg
XM_005247389.4:c.953A>G XP_005247446.1:p.His318Arg
XM_011512738.2:c.1049A>G XP_011511040.1:p.His350Arg
XM_011512739.2:c.512A>G XP_011511041.1:p.His171Arg
NM_001199799.2:c.1049A>G MANE Select NP_001186728.1:p.His350Arg
NM_001199800.2:c.782A>G NP_001186729.1:p.His261Arg
NM_175924.4:c.917A>G NP_787120.1:p.His306Arg