Canonical Allele Identifier: CA412150473
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489811C>T , CM000684.2:g.50489811C>T GRCh38
NC_000022.10:g.50928240C>T , CM000684.1:g.50928240C>T GRCh37
NC_000022.9:g.49275106C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.813C>T MANE Select ENSP00000216075.6:p.Tyr271=
ENST00000216075.10:c.813C>T ENSP00000216075.6:p.Tyr271=
ENST00000395732.7:c.799C>T ENSP00000379081.3:p.Pro267Ser
ENST00000395733.7:c.682C>T ENSP00000379082.3:p.Pro228Ser
ENST00000451761.1:c.753C>T ENSP00000409894.1:p.Tyr251=
NM_017584.5:c.813C>T NP_060054.4:p.Tyr271=
XM_005261925.3:c.675C>T XP_005261982.1:p.Tyr225=
XR_244455.2:n.3309C>T
XM_005261925.4:c.675C>T XP_005261982.1:p.Tyr225=
NM_017584.6:c.813C>T MANE Select NP_060054.4:p.Tyr271=