Canonical Allele Identifier: CA354143935
Gene: ILDR1 HGNC NCBI

Linked Data

dbSNP Id: rs751310993

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993662C>A , CM000665.2:g.121993662C>A GRCh38
NC_000003.11:g.121712509C>A , CM000665.1:g.121712509C>A GRCh37
NC_000003.10:g.123195199C>A NCBI36
NG_031870.1:g.33619G>T
NG_031870.2:g.71893G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1087G>T MANE Select ENSP00000345667.5:p.Asp363Tyr
ENST00000460554.2:n.1037G>T
ENST00000642615.1:c.*270G>T ENSP00000495499.1:n.*270G>T
ENST00000273691.7:c.955G>T ENSP00000273691.3:p.Asp319Tyr
ENST00000344209.9:c.1087G>T ENSP00000345667.5:p.Asp363Tyr
ENST00000393631.5:c.820G>T ENSP00000377251.1:p.Asp274Tyr
ENST00000460554.1:n.1189G>T
ENST00000462014.1:c.991G>T ENSP00000419414.1:p.Asp331Tyr
NM_001199799.1:c.1087G>T NP_001186728.1:p.Asp363Tyr
NM_001199800.1:c.820G>T NP_001186729.1:p.Asp274Tyr
NM_175924.3:c.955G>T NP_787120.1:p.Asp319Tyr
XM_005247389.3:c.991G>T XP_005247446.1:p.Asp331Tyr
XM_011512738.1:c.1087G>T XP_011511040.1:p.Asp363Tyr
XM_011512739.1:c.550G>T XP_011511041.1:p.Asp184Tyr
XM_005247389.4:c.991G>T XP_005247446.1:p.Asp331Tyr
XM_011512738.2:c.1087G>T XP_011511040.1:p.Asp363Tyr
XM_011512739.2:c.550G>T XP_011511041.1:p.Asp184Tyr
NM_001199799.2:c.1087G>T MANE Select NP_001186728.1:p.Asp363Tyr
NM_001199800.2:c.820G>T NP_001186729.1:p.Asp274Tyr
NM_175924.4:c.955G>T NP_787120.1:p.Asp319Tyr