Canonical Allele Identifier: CA412150481
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489813A>T , CM000684.2:g.50489813A>T GRCh38
NC_000022.10:g.50928242A>T , CM000684.1:g.50928242A>T GRCh37
NC_000022.9:g.49275108A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.815A>T MANE Select ENSP00000216075.6:p.Gln272Leu
ENST00000216075.10:c.815A>T ENSP00000216075.6:p.Gln272Leu
ENST00000395732.7:c.801A>T ENSP00000379081.3:p.Pro267=
ENST00000395733.7:c.684A>T ENSP00000379082.3:p.Pro228=
ENST00000451761.1:c.755A>T ENSP00000409894.1:p.Gln252Leu
NM_017584.5:c.815A>T NP_060054.4:p.Gln272Leu
XM_005261925.3:c.677A>T XP_005261982.1:p.Gln226Leu
XR_244455.2:n.3311A>T
XM_005261925.4:c.677A>T XP_005261982.1:p.Gln226Leu
NM_017584.6:c.815A>T MANE Select NP_060054.4:p.Gln272Leu