Canonical Allele Identifier: CA2568667
Gene: ILDR1 HGNC NCBI

Linked Data

dbSNP Id: rs775302314

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993276G>A , CM000665.2:g.121993276G>A GRCh38
NC_000003.11:g.121712123G>A , CM000665.1:g.121712123G>A GRCh37
NC_000003.10:g.123194813G>A NCBI36
NG_031870.1:g.34005C>T
NG_031870.2:g.72279C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1473C>T MANE Select ENSP00000345667.5:p.Ser491=
ENST00000460554.2:n.1423C>T
ENST00000642615.1:c.*656C>T ENSP00000495499.1:n.*656C>T
ENST00000273691.7:c.1341C>T ENSP00000273691.3:p.Ser447=
ENST00000344209.9:c.1473C>T ENSP00000345667.5:p.Ser491=
ENST00000393631.5:c.1206C>T ENSP00000377251.1:p.Ser402=
ENST00000460554.1:n.1575C>T
ENST00000462014.1:c.1377C>T ENSP00000419414.1:p.Ser459=
NM_001199799.1:c.1473C>T NP_001186728.1:p.Ser491=
NM_001199800.1:c.1206C>T NP_001186729.1:p.Ser402=
NM_175924.3:c.1341C>T NP_787120.1:p.Ser447=
XM_005247389.3:c.1377C>T XP_005247446.1:p.Ser459=
XM_011512738.1:c.1473C>T XP_011511040.1:p.Ser491=
XM_011512739.1:c.936C>T XP_011511041.1:p.Ser312=
XM_005247389.4:c.1377C>T XP_005247446.1:p.Ser459=
XM_011512738.2:c.1473C>T XP_011511040.1:p.Ser491=
XM_011512739.2:c.936C>T XP_011511041.1:p.Ser312=
NM_001199799.2:c.1473C>T MANE Select NP_001186728.1:p.Ser491=
NM_001199800.2:c.1206C>T NP_001186729.1:p.Ser402=
NM_175924.4:c.1341C>T NP_787120.1:p.Ser447=