Canonical Allele Identifier: CA354143504
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993576T>G , CM000665.2:g.121993576T>G GRCh38
NC_000003.11:g.121712423T>G , CM000665.1:g.121712423T>G GRCh37
NC_000003.10:g.123195113T>G NCBI36
NG_031870.1:g.33705A>C
NG_031870.2:g.71979A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1173A>C MANE Select ENSP00000345667.5:p.Glu391Asp
ENST00000460554.2:n.1123A>C
ENST00000642615.1:c.*356A>C ENSP00000495499.1:n.*356A>C
ENST00000273691.7:c.1041A>C ENSP00000273691.3:p.Glu347Asp
ENST00000344209.9:c.1173A>C ENSP00000345667.5:p.Glu391Asp
ENST00000393631.5:c.906A>C ENSP00000377251.1:p.Glu302Asp
ENST00000460554.1:n.1275A>C
ENST00000462014.1:c.1077A>C ENSP00000419414.1:p.Glu359Asp
NM_001199799.1:c.1173A>C NP_001186728.1:p.Glu391Asp
NM_001199800.1:c.906A>C NP_001186729.1:p.Glu302Asp
NM_175924.3:c.1041A>C NP_787120.1:p.Glu347Asp
XM_005247389.3:c.1077A>C XP_005247446.1:p.Glu359Asp
XM_011512738.1:c.1173A>C XP_011511040.1:p.Glu391Asp
XM_011512739.1:c.636A>C XP_011511041.1:p.Glu212Asp
XM_005247389.4:c.1077A>C XP_005247446.1:p.Glu359Asp
XM_011512738.2:c.1173A>C XP_011511040.1:p.Glu391Asp
XM_011512739.2:c.636A>C XP_011511041.1:p.Glu212Asp
NM_001199799.2:c.1173A>C MANE Select NP_001186728.1:p.Glu391Asp
NM_001199800.2:c.906A>C NP_001186729.1:p.Glu302Asp
NM_175924.4:c.1041A>C NP_787120.1:p.Glu347Asp