Canonical Allele Identifier: CA435423827
Gene: ILDR1 HGNC NCBI

Linked Data

dbSNP Id: rs1308259269

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993648C>T , CM000665.2:g.121993648C>T GRCh38
NC_000003.11:g.121712495C>T , CM000665.1:g.121712495C>T GRCh37
NC_000003.10:g.123195185C>T NCBI36
NG_031870.1:g.33633G>A
NG_031870.2:g.71907G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1101G>A MANE Select ENSP00000345667.5:p.Gly367=
ENST00000460554.2:n.1051G>A
ENST00000642615.1:c.*284G>A ENSP00000495499.1:n.*284G>A
ENST00000273691.7:c.969G>A ENSP00000273691.3:p.Gly323=
ENST00000344209.9:c.1101G>A ENSP00000345667.5:p.Gly367=
ENST00000393631.5:c.834G>A ENSP00000377251.1:p.Gly278=
ENST00000460554.1:n.1203G>A
ENST00000462014.1:c.1005G>A ENSP00000419414.1:p.Gly335=
NM_001199799.1:c.1101G>A NP_001186728.1:p.Gly367=
NM_001199800.1:c.834G>A NP_001186729.1:p.Gly278=
NM_175924.3:c.969G>A NP_787120.1:p.Gly323=
XM_005247389.3:c.1005G>A XP_005247446.1:p.Gly335=
XM_011512738.1:c.1101G>A XP_011511040.1:p.Gly367=
XM_011512739.1:c.564G>A XP_011511041.1:p.Gly188=
XM_005247389.4:c.1005G>A XP_005247446.1:p.Gly335=
XM_011512738.2:c.1101G>A XP_011511040.1:p.Gly367=
XM_011512739.2:c.564G>A XP_011511041.1:p.Gly188=
NM_001199799.2:c.1101G>A MANE Select NP_001186728.1:p.Gly367=
NM_001199800.2:c.834G>A NP_001186729.1:p.Gly278=
NM_175924.4:c.969G>A NP_787120.1:p.Gly323=