Canonical Allele Identifier: CA354143913
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993652T>G , CM000665.2:g.121993652T>G GRCh38
NC_000003.11:g.121712499T>G , CM000665.1:g.121712499T>G GRCh37
NC_000003.10:g.123195189T>G NCBI36
NG_031870.1:g.33629A>C
NG_031870.2:g.71903A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1097A>C MANE Select ENSP00000345667.5:p.Glu366Ala
ENST00000460554.2:n.1047A>C
ENST00000642615.1:c.*280A>C ENSP00000495499.1:n.*280A>C
ENST00000273691.7:c.965A>C ENSP00000273691.3:p.Glu322Ala
ENST00000344209.9:c.1097A>C ENSP00000345667.5:p.Glu366Ala
ENST00000393631.5:c.830A>C ENSP00000377251.1:p.Glu277Ala
ENST00000460554.1:n.1199A>C
ENST00000462014.1:c.1001A>C ENSP00000419414.1:p.Glu334Ala
NM_001199799.1:c.1097A>C NP_001186728.1:p.Glu366Ala
NM_001199800.1:c.830A>C NP_001186729.1:p.Glu277Ala
NM_175924.3:c.965A>C NP_787120.1:p.Glu322Ala
XM_005247389.3:c.1001A>C XP_005247446.1:p.Glu334Ala
XM_011512738.1:c.1097A>C XP_011511040.1:p.Glu366Ala
XM_011512739.1:c.560A>C XP_011511041.1:p.Glu187Ala
XM_005247389.4:c.1001A>C XP_005247446.1:p.Glu334Ala
XM_011512738.2:c.1097A>C XP_011511040.1:p.Glu366Ala
XM_011512739.2:c.560A>C XP_011511041.1:p.Glu187Ala
NM_001199799.2:c.1097A>C MANE Select NP_001186728.1:p.Glu366Ala
NM_001199800.2:c.830A>C NP_001186729.1:p.Glu277Ala
NM_175924.4:c.965A>C NP_787120.1:p.Glu322Ala