Canonical Allele Identifier: CA354143430
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993557A>G , CM000665.2:g.121993557A>G GRCh38
NC_000003.11:g.121712404A>G , CM000665.1:g.121712404A>G GRCh37
NC_000003.10:g.123195094A>G NCBI36
NG_031870.1:g.33724T>C
NG_031870.2:g.71998T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1192T>C MANE Select ENSP00000345667.5:p.Ser398Pro
ENST00000460554.2:n.1142T>C
ENST00000642615.1:c.*375T>C ENSP00000495499.1:n.*375T>C
ENST00000273691.7:c.1060T>C ENSP00000273691.3:p.Ser354Pro
ENST00000344209.9:c.1192T>C ENSP00000345667.5:p.Ser398Pro
ENST00000393631.5:c.925T>C ENSP00000377251.1:p.Ser309Pro
ENST00000460554.1:n.1294T>C
ENST00000462014.1:c.1096T>C ENSP00000419414.1:p.Ser366Pro
NM_001199799.1:c.1192T>C NP_001186728.1:p.Ser398Pro
NM_001199800.1:c.925T>C NP_001186729.1:p.Ser309Pro
NM_175924.3:c.1060T>C NP_787120.1:p.Ser354Pro
XM_005247389.3:c.1096T>C XP_005247446.1:p.Ser366Pro
XM_011512738.1:c.1192T>C XP_011511040.1:p.Ser398Pro
XM_011512739.1:c.655T>C XP_011511041.1:p.Ser219Pro
XM_005247389.4:c.1096T>C XP_005247446.1:p.Ser366Pro
XM_011512738.2:c.1192T>C XP_011511040.1:p.Ser398Pro
XM_011512739.2:c.655T>C XP_011511041.1:p.Ser219Pro
NM_001199799.2:c.1192T>C MANE Select NP_001186728.1:p.Ser398Pro
NM_001199800.2:c.925T>C NP_001186729.1:p.Ser309Pro
NM_175924.4:c.1060T>C NP_787120.1:p.Ser354Pro