Canonical Allele Identifier: CA1397750680
Gene: ILDR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993172T= , CM000665.2:g.121993172T= GRCh38
NC_000003.11:g.121712019T= , CM000665.1:g.121712019T= GRCh37
NC_000003.10:g.123194709T= NCBI36
NG_031870.1:g.34109A=
NG_031870.2:g.72383A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1577A= MANE Select ENSP00000345667.5:p.Lys526=
ENST00000460554.2:n.1527A=
ENST00000642615.1:c.*760A= ENSP00000495499.1:n.*760A=
ENST00000273691.7:c.1445A= ENSP00000273691.3:p.Lys482=
ENST00000344209.9:c.1577A= ENSP00000345667.5:p.Lys526=
ENST00000393631.5:c.1310A= ENSP00000377251.1:p.Lys437=
ENST00000460554.1:n.1679A=
ENST00000462014.1:c.1481A= ENSP00000419414.1:p.Lys494=
NM_001199799.1:c.1577A= NP_001186728.1:p.Lys526=
NM_001199800.1:c.1310A= NP_001186729.1:p.Lys437=
NM_175924.3:c.1445A= NP_787120.1:p.Lys482=
XM_005247389.3:c.1481A= XP_005247446.1:p.Lys494=
XM_011512738.1:c.1558+19A= XP_011511040.1:n.1558+19A=
XM_011512739.1:c.1040A= XP_011511041.1:p.Lys347=
XM_005247389.4:c.1481A= XP_005247446.1:p.Lys494=
XM_011512738.2:c.1558+19A= XP_011511040.1:n.1558+19A=
XM_011512739.2:c.1040A= XP_011511041.1:p.Lys347=
NM_001199799.2:c.1577A= MANE Select NP_001186728.1:p.Lys526=
NM_001199800.2:c.1310A= NP_001186729.1:p.Lys437=
NM_175924.4:c.1445A= NP_787120.1:p.Lys482=