Canonical Allele Identifier: CA1397750778
Gene: ILDR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993352C= , CM000665.2:g.121993352C= GRCh38
NC_000003.11:g.121712199C= , CM000665.1:g.121712199C= GRCh37
NC_000003.10:g.123194889C= NCBI36
NG_031870.1:g.33929G=
NG_031870.2:g.72203G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1397G= MANE Select ENSP00000345667.5:p.Arg466=
ENST00000460554.2:n.1347G=
ENST00000642615.1:c.*580G= ENSP00000495499.1:n.*580G=
ENST00000273691.7:c.1265G= ENSP00000273691.3:p.Arg422=
ENST00000344209.9:c.1397G= ENSP00000345667.5:p.Arg466=
ENST00000393631.5:c.1130G= ENSP00000377251.1:p.Arg377=
ENST00000460554.1:n.1499G=
ENST00000462014.1:c.1301G= ENSP00000419414.1:p.Arg434=
NM_001199799.1:c.1397G= NP_001186728.1:p.Arg466=
NM_001199800.1:c.1130G= NP_001186729.1:p.Arg377=
NM_175924.3:c.1265G= NP_787120.1:p.Arg422=
XM_005247389.3:c.1301G= XP_005247446.1:p.Arg434=
XM_011512738.1:c.1397G= XP_011511040.1:p.Arg466=
XM_011512739.1:c.860G= XP_011511041.1:p.Arg287=
XM_005247389.4:c.1301G= XP_005247446.1:p.Arg434=
XM_011512738.2:c.1397G= XP_011511040.1:p.Arg466=
XM_011512739.2:c.860G= XP_011511041.1:p.Arg287=
NM_001199799.2:c.1397G= MANE Select NP_001186728.1:p.Arg466=
NM_001199800.2:c.1130G= NP_001186729.1:p.Arg377=
NM_175924.4:c.1265G= NP_787120.1:p.Arg422=