Canonical Allele Identifier: CA354143350
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993534G>T , CM000665.2:g.121993534G>T GRCh38
NC_000003.11:g.121712381G>T , CM000665.1:g.121712381G>T GRCh37
NC_000003.10:g.123195071G>T NCBI36
NG_031870.1:g.33747C>A
NG_031870.2:g.72021C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1215C>A MANE Select ENSP00000345667.5:p.Ser405Arg
ENST00000460554.2:n.1165C>A
ENST00000642615.1:c.*398C>A ENSP00000495499.1:n.*398C>A
ENST00000273691.7:c.1083C>A ENSP00000273691.3:p.Ser361Arg
ENST00000344209.9:c.1215C>A ENSP00000345667.5:p.Ser405Arg
ENST00000393631.5:c.948C>A ENSP00000377251.1:p.Ser316Arg
ENST00000460554.1:n.1317C>A
ENST00000462014.1:c.1119C>A ENSP00000419414.1:p.Ser373Arg
NM_001199799.1:c.1215C>A NP_001186728.1:p.Ser405Arg
NM_001199800.1:c.948C>A NP_001186729.1:p.Ser316Arg
NM_175924.3:c.1083C>A NP_787120.1:p.Ser361Arg
XM_005247389.3:c.1119C>A XP_005247446.1:p.Ser373Arg
XM_011512738.1:c.1215C>A XP_011511040.1:p.Ser405Arg
XM_011512739.1:c.678C>A XP_011511041.1:p.Ser226Arg
XM_005247389.4:c.1119C>A XP_005247446.1:p.Ser373Arg
XM_011512738.2:c.1215C>A XP_011511040.1:p.Ser405Arg
XM_011512739.2:c.678C>A XP_011511041.1:p.Ser226Arg
NM_001199799.2:c.1215C>A MANE Select NP_001186728.1:p.Ser405Arg
NM_001199800.2:c.948C>A NP_001186729.1:p.Ser316Arg
NM_175924.4:c.1083C>A NP_787120.1:p.Ser361Arg