Canonical Allele Identifier: CA1397750780
Gene: ILDR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.121993355T= , CM000665.2:g.121993355T= GRCh38
NC_000003.11:g.121712202T= , CM000665.1:g.121712202T= GRCh37
NC_000003.10:g.123194892T= NCBI36
NG_031870.1:g.33926A=
NG_031870.2:g.72200A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000344209.10:c.1394A= MANE Select ENSP00000345667.5:p.His465=
ENST00000460554.2:n.1344A=
ENST00000642615.1:c.*577A= ENSP00000495499.1:n.*577A=
ENST00000273691.7:c.1262A= ENSP00000273691.3:p.His421=
ENST00000344209.9:c.1394A= ENSP00000345667.5:p.His465=
ENST00000393631.5:c.1127A= ENSP00000377251.1:p.His376=
ENST00000460554.1:n.1496A=
ENST00000462014.1:c.1298A= ENSP00000419414.1:p.His433=
NM_001199799.1:c.1394A= NP_001186728.1:p.His465=
NM_001199800.1:c.1127A= NP_001186729.1:p.His376=
NM_175924.3:c.1262A= NP_787120.1:p.His421=
XM_005247389.3:c.1298A= XP_005247446.1:p.His433=
XM_011512738.1:c.1394A= XP_011511040.1:p.His465=
XM_011512739.1:c.857A= XP_011511041.1:p.His286=
XM_005247389.4:c.1298A= XP_005247446.1:p.His433=
XM_011512738.2:c.1394A= XP_011511040.1:p.His465=
XM_011512739.2:c.857A= XP_011511041.1:p.His286=
NM_001199799.2:c.1394A= MANE Select NP_001186728.1:p.His465=
NM_001199800.2:c.1127A= NP_001186729.1:p.His376=
NM_175924.4:c.1262A= NP_787120.1:p.His421=