Canonical Allele Identifier: CA1397750844
Gene: ILDR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993457C= , CM000665.2:g.121993457C= GRCh38
NC_000003.11:g.121712304C= , CM000665.1:g.121712304C= GRCh37
NC_000003.10:g.123194994C= NCBI36
NG_031870.1:g.33824G=
NG_031870.2:g.72098G=

Transcript Alleles

HGVS Amino-acid change
ENST00000344209.10:c.1292G= MANE Select ENSP00000345667.5:p.Arg431=
ENST00000460554.2:n.1242G=
ENST00000642615.1:c.*475G= ENSP00000495499.1:n.*475G=
ENST00000273691.7:c.1160G= ENSP00000273691.3:p.Arg387=
ENST00000344209.9:c.1292G= ENSP00000345667.5:p.Arg431=
ENST00000393631.5:c.1025G= ENSP00000377251.1:p.Arg342=
ENST00000460554.1:n.1394G=
ENST00000462014.1:c.1196G= ENSP00000419414.1:p.Arg399=
NM_001199799.1:c.1292G= NP_001186728.1:p.Arg431=
NM_001199800.1:c.1025G= NP_001186729.1:p.Arg342=
NM_175924.3:c.1160G= NP_787120.1:p.Arg387=
XM_005247389.3:c.1196G= XP_005247446.1:p.Arg399=
XM_011512738.1:c.1292G= XP_011511040.1:p.Arg431=
XM_011512739.1:c.755G= XP_011511041.1:p.Arg252=
XM_005247389.4:c.1196G= XP_005247446.1:p.Arg399=
XM_011512738.2:c.1292G= XP_011511040.1:p.Arg431=
XM_011512739.2:c.755G= XP_011511041.1:p.Arg252=
NM_001199799.2:c.1292G= MANE Select NP_001186728.1:p.Arg431=
NM_001199800.2:c.1025G= NP_001186729.1:p.Arg342=
NM_175924.4:c.1160G= NP_787120.1:p.Arg387=