Canonical Allele Identifier: CA435423706
Gene: ILDR1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.121712099C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993252C>G , CM000665.2:g.121993252C>G GRCh38
NC_000003.11:g.121712099C>G , CM000665.1:g.121712099C>G GRCh37
NC_000003.10:g.123194789C>G NCBI36
NG_031870.1:g.34029G>C
NG_031870.2:g.72303G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1497G>C MANE Select ENSP00000345667.5:p.Ser499=
ENST00000460554.2:n.1447G>C
ENST00000642615.1:c.*680G>C ENSP00000495499.1:n.*680G>C
ENST00000273691.7:c.1365G>C ENSP00000273691.3:p.Ser455=
ENST00000344209.9:c.1497G>C ENSP00000345667.5:p.Ser499=
ENST00000393631.5:c.1230G>C ENSP00000377251.1:p.Ser410=
ENST00000460554.1:n.1599G>C
ENST00000462014.1:c.1401G>C ENSP00000419414.1:p.Ser467=
NM_001199799.1:c.1497G>C NP_001186728.1:p.Ser499=
NM_001199800.1:c.1230G>C NP_001186729.1:p.Ser410=
NM_175924.3:c.1365G>C NP_787120.1:p.Ser455=
XM_005247389.3:c.1401G>C XP_005247446.1:p.Ser467=
XM_011512738.1:c.1497G>C XP_011511040.1:p.Ser499=
XM_011512739.1:c.960G>C XP_011511041.1:p.Ser320=
XM_005247389.4:c.1401G>C XP_005247446.1:p.Ser467=
XM_011512738.2:c.1497G>C XP_011511040.1:p.Ser499=
XM_011512739.2:c.960G>C XP_011511041.1:p.Ser320=
NM_001199799.2:c.1497G>C MANE Select NP_001186728.1:p.Ser499=
NM_001199800.2:c.1230G>C NP_001186729.1:p.Ser410=
NM_175924.4:c.1365G>C NP_787120.1:p.Ser455=