Canonical Allele Identifier: CA354144033
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993708G>T , CM000665.2:g.121993708G>T GRCh38
NC_000003.11:g.121712555G>T , CM000665.1:g.121712555G>T GRCh37
NC_000003.10:g.123195245G>T NCBI36
NG_031870.1:g.33573C>A
NG_031870.2:g.71847C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1041C>A MANE Select ENSP00000345667.5:p.Asp347Glu
ENST00000460554.2:n.991C>A
ENST00000642615.1:c.*224C>A ENSP00000495499.1:n.*224C>A
ENST00000273691.7:c.909C>A ENSP00000273691.3:p.Asp303Glu
ENST00000344209.9:c.1041C>A ENSP00000345667.5:p.Asp347Glu
ENST00000393631.5:c.774C>A ENSP00000377251.1:p.Asp258Glu
ENST00000460554.1:n.1143C>A
ENST00000462014.1:c.945C>A ENSP00000419414.1:p.Asp315Glu
NM_001199799.1:c.1041C>A NP_001186728.1:p.Asp347Glu
NM_001199800.1:c.774C>A NP_001186729.1:p.Asp258Glu
NM_175924.3:c.909C>A NP_787120.1:p.Asp303Glu
XM_005247389.3:c.945C>A XP_005247446.1:p.Asp315Glu
XM_011512738.1:c.1041C>A XP_011511040.1:p.Asp347Glu
XM_011512739.1:c.504C>A XP_011511041.1:p.Asp168Glu
XM_005247389.4:c.945C>A XP_005247446.1:p.Asp315Glu
XM_011512738.2:c.1041C>A XP_011511040.1:p.Asp347Glu
XM_011512739.2:c.504C>A XP_011511041.1:p.Asp168Glu
NM_001199799.2:c.1041C>A MANE Select NP_001186728.1:p.Asp347Glu
NM_001199800.2:c.774C>A NP_001186729.1:p.Asp258Glu
NM_175924.4:c.909C>A NP_787120.1:p.Asp303Glu