Canonical Allele Identifier: CA515385220
Gene: MIOX HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.50928258G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489829G>A , CM000684.2:g.50489829G>A GRCh38
NC_000022.10:g.50928258G>A , CM000684.1:g.50928258G>A GRCh37
NC_000022.9:g.49275124G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000216075.11:c.831G>A MANE Select ENSP00000216075.6:p.Lys277=
ENST00000216075.10:c.831G>A ENSP00000216075.6:p.Lys277=
ENST00000395732.7:c.*4G>A ENSP00000379081.3:n.*4G>A
ENST00000395733.7:c.*4G>A ENSP00000379082.3:n.*4G>A
ENST00000451761.1:c.771G>A ENSP00000409894.1:p.Lys257=
NM_017584.5:c.831G>A NP_060054.4:p.Lys277=
XM_005261925.3:c.693G>A XP_005261982.1:p.Lys231=
XR_244455.2:n.3327G>A
XM_005261925.4:c.693G>A XP_005261982.1:p.Lys231=
NM_017584.6:c.831G>A MANE Select NP_060054.4:p.Lys277=