Canonical Allele Identifier: CA2410885408
Gene: MIOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489929C= , CM000684.2:g.50489929C= GRCh38
NC_000022.10:g.50928358C= , CM000684.1:g.50928358C= GRCh37
NC_000022.9:g.49275224C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.*73C= MANE Select ENSP00000216075.6:n.*73C=
ENST00000216075.10:c.*73C= ENSP00000216075.6:n.*73C=
ENST00000395732.7:c.*104C= ENSP00000379081.3:n.*104C=
ENST00000395733.7:c.*104C= ENSP00000379082.3:n.*104C=
ENST00000451761.1:c.871C= ENSP00000409894.1:n.871C=
NM_017584.5:c.*73C= NP_060054.4:n.*73C=
XM_005261925.3:c.*73C= XP_005261982.1:n.*73C=
XR_244455.2:n.3427C=
XM_005261925.4:c.*73C= XP_005261982.1:n.*73C=
NM_017584.6:c.*73C= MANE Select NP_060054.4:n.*73C=