Canonical Allele Identifier: CA412150522
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489820C>G , CM000684.2:g.50489820C>G GRCh38
NC_000022.10:g.50928249C>G , CM000684.1:g.50928249C>G GRCh37
NC_000022.9:g.49275115C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.822C>G MANE Select ENSP00000216075.6:p.Leu274=
ENST00000216075.10:c.822C>G ENSP00000216075.6:p.Leu274=
ENST00000395732.7:c.808C>G ENSP00000379081.3:p.His270Asp
ENST00000395733.7:c.691C>G ENSP00000379082.3:p.His231Asp
ENST00000451761.1:c.762C>G ENSP00000409894.1:p.Leu254=
NM_017584.5:c.822C>G NP_060054.4:p.Leu274=
XM_005261925.3:c.684C>G XP_005261982.1:p.Leu228=
XR_244455.2:n.3318C>G
XM_005261925.4:c.684C>G XP_005261982.1:p.Leu228=
NM_017584.6:c.822C>G MANE Select NP_060054.4:p.Leu274=