Canonical Allele Identifier: CA354143895
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993644T>G , CM000665.2:g.121993644T>G GRCh38
NC_000003.11:g.121712491T>G , CM000665.1:g.121712491T>G GRCh37
NC_000003.10:g.123195181T>G NCBI36
NG_031870.1:g.33637A>C
NG_031870.2:g.71911A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1105A>C MANE Select ENSP00000345667.5:p.Ser369Arg
ENST00000460554.2:n.1055A>C
ENST00000642615.1:c.*288A>C ENSP00000495499.1:n.*288A>C
ENST00000273691.7:c.973A>C ENSP00000273691.3:p.Ser325Arg
ENST00000344209.9:c.1105A>C ENSP00000345667.5:p.Ser369Arg
ENST00000393631.5:c.838A>C ENSP00000377251.1:p.Ser280Arg
ENST00000460554.1:n.1207A>C
ENST00000462014.1:c.1009A>C ENSP00000419414.1:p.Ser337Arg
NM_001199799.1:c.1105A>C NP_001186728.1:p.Ser369Arg
NM_001199800.1:c.838A>C NP_001186729.1:p.Ser280Arg
NM_175924.3:c.973A>C NP_787120.1:p.Ser325Arg
XM_005247389.3:c.1009A>C XP_005247446.1:p.Ser337Arg
XM_011512738.1:c.1105A>C XP_011511040.1:p.Ser369Arg
XM_011512739.1:c.568A>C XP_011511041.1:p.Ser190Arg
XM_005247389.4:c.1009A>C XP_005247446.1:p.Ser337Arg
XM_011512738.2:c.1105A>C XP_011511040.1:p.Ser369Arg
XM_011512739.2:c.568A>C XP_011511041.1:p.Ser190Arg
NM_001199799.2:c.1105A>C MANE Select NP_001186728.1:p.Ser369Arg
NM_001199800.2:c.838A>C NP_001186729.1:p.Ser280Arg
NM_175924.4:c.973A>C NP_787120.1:p.Ser325Arg