Canonical Allele Identifier: CA354143227
Gene: ILDR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993497T>A , CM000665.2:g.121993497T>A GRCh38
NC_000003.11:g.121712344T>A , CM000665.1:g.121712344T>A GRCh37
NC_000003.10:g.123195034T>A NCBI36
NG_031870.1:g.33784A>T
NG_031870.2:g.72058A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000344209.10:c.1252A>T MANE Select ENSP00000345667.5:p.Arg418Trp
ENST00000460554.2:n.1202A>T
ENST00000642615.1:c.*435A>T ENSP00000495499.1:n.*435A>T
ENST00000273691.7:c.1120A>T ENSP00000273691.3:p.Arg374Trp
ENST00000344209.9:c.1252A>T ENSP00000345667.5:p.Arg418Trp
ENST00000393631.5:c.985A>T ENSP00000377251.1:p.Arg329Trp
ENST00000460554.1:n.1354A>T
ENST00000462014.1:c.1156A>T ENSP00000419414.1:p.Arg386Trp
NM_001199799.1:c.1252A>T NP_001186728.1:p.Arg418Trp
NM_001199800.1:c.985A>T NP_001186729.1:p.Arg329Trp
NM_175924.3:c.1120A>T NP_787120.1:p.Arg374Trp
XM_005247389.3:c.1156A>T XP_005247446.1:p.Arg386Trp
XM_011512738.1:c.1252A>T XP_011511040.1:p.Arg418Trp
XM_011512739.1:c.715A>T XP_011511041.1:p.Arg239Trp
XM_005247389.4:c.1156A>T XP_005247446.1:p.Arg386Trp
XM_011512738.2:c.1252A>T XP_011511040.1:p.Arg418Trp
XM_011512739.2:c.715A>T XP_011511041.1:p.Arg239Trp
NM_001199799.2:c.1252A>T MANE Select NP_001186728.1:p.Arg418Trp
NM_001199800.2:c.985A>T NP_001186729.1:p.Arg329Trp
NM_175924.4:c.1120A>T NP_787120.1:p.Arg374Trp