Canonical Allele Identifier: CA412150527
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489821A>G , CM000684.2:g.50489821A>G GRCh38
NC_000022.10:g.50928250A>G , CM000684.1:g.50928250A>G GRCh37
NC_000022.9:g.49275116A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.823A>G MANE Select ENSP00000216075.6:p.Ile275Val
ENST00000216075.10:c.823A>G ENSP00000216075.6:p.Ile275Val
ENST00000395732.7:c.809A>G ENSP00000379081.3:p.His270Arg
ENST00000395733.7:c.692A>G ENSP00000379082.3:p.His231Arg
ENST00000451761.1:c.763A>G ENSP00000409894.1:p.Ile255Val
NM_017584.5:c.823A>G NP_060054.4:p.Ile275Val
XM_005261925.3:c.685A>G XP_005261982.1:p.Ile229Val
XR_244455.2:n.3319A>G
XM_005261925.4:c.685A>G XP_005261982.1:p.Ile229Val
NM_017584.6:c.823A>G MANE Select NP_060054.4:p.Ile275Val