Canonical Allele Identifier: CA412150580

Gene: MIOX

Linked Data

• MyVariant Identifiers: chr22:g.50928254A>G (hg19) ; chr22:g.50489825A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50489825A>G , CM000684.2:g.50489825A>G	GRCh38
NC_000022.10:g.50928254A>G , CM000684.1:g.50928254A>G	GRCh37
NC_000022.9:g.49275120A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216075.11:c.827A>G MANE Select	ENSP00000216075.6:p.Asp276Gly
ENST00000216075.10:c.827A>G	ENSP00000216075.6:p.Asp276Gly
ENST00000395732.7:c.813A>G	ENSP00000379081.3:p.Ter271Trp
ENST00000395733.7:c.696A>G	ENSP00000379082.3:p.Ter232Trp
ENST00000451761.1:c.767A>G	ENSP00000409894.1:p.Asp256Gly
NM_017584.5:c.827A>G	NP_060054.4:p.Asp276Gly
XM_005261925.3:c.689A>G	XP_005261982.1:p.Asp230Gly
XR_244455.2:n.3323A>G
XM_005261925.4:c.689A>G	XP_005261982.1:p.Asp230Gly
NM_017584.6:c.827A>G MANE Select	NP_060054.4:p.Asp276Gly