Canonical Allele Identifier: CA1397750842
Gene: ILDR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993455A= , CM000665.2:g.121993455A= GRCh38
NC_000003.11:g.121712302A= , CM000665.1:g.121712302A= GRCh37
NC_000003.10:g.123194992A= NCBI36
NG_031870.1:g.33826T=
NG_031870.2:g.72100T=

Transcript Alleles

HGVS Amino-acid change
ENST00000344209.10:c.1294T= MANE Select ENSP00000345667.5:p.Trp432=
ENST00000460554.2:n.1244T=
ENST00000642615.1:c.*477T= ENSP00000495499.1:n.*477T=
ENST00000273691.7:c.1162T= ENSP00000273691.3:p.Trp388=
ENST00000344209.9:c.1294T= ENSP00000345667.5:p.Trp432=
ENST00000393631.5:c.1027T= ENSP00000377251.1:p.Trp343=
ENST00000460554.1:n.1396T=
ENST00000462014.1:c.1198T= ENSP00000419414.1:p.Trp400=
NM_001199799.1:c.1294T= NP_001186728.1:p.Trp432=
NM_001199800.1:c.1027T= NP_001186729.1:p.Trp343=
NM_175924.3:c.1162T= NP_787120.1:p.Trp388=
XM_005247389.3:c.1198T= XP_005247446.1:p.Trp400=
XM_011512738.1:c.1294T= XP_011511040.1:p.Trp432=
XM_011512739.1:c.757T= XP_011511041.1:p.Trp253=
XM_005247389.4:c.1198T= XP_005247446.1:p.Trp400=
XM_011512738.2:c.1294T= XP_011511040.1:p.Trp432=
XM_011512739.2:c.757T= XP_011511041.1:p.Trp253=
NM_001199799.2:c.1294T= MANE Select NP_001186728.1:p.Trp432=
NM_001199800.2:c.1027T= NP_001186729.1:p.Trp343=
NM_175924.4:c.1162T= NP_787120.1:p.Trp388=