Canonical Allele Identifier: CA412150524
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.823A>C MANE Select ENSP00000216075.6:p.Ile275Leu
ENST00000216075.10:c.823A>C ENSP00000216075.6:p.Ile275Leu
ENST00000395732.7:c.809A>C ENSP00000379081.3:p.His270Pro
ENST00000395733.7:c.692A>C ENSP00000379082.3:p.His231Pro
ENST00000451761.1:c.763A>C ENSP00000409894.1:p.Ile255Leu
NM_017584.5:c.823A>C NP_060054.4:p.Ile275Leu
XM_005261925.3:c.685A>C XP_005261982.1:p.Ile229Leu
XR_244455.2:n.3319A>C
XM_005261925.4:c.685A>C XP_005261982.1:p.Ile229Leu
NM_017584.6:c.823A>C MANE Select NP_060054.4:p.Ile275Leu