Canonical Allele Identifier: CA412150476
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489812C>A , CM000684.2:g.50489812C>A GRCh38
NC_000022.10:g.50928241C>A , CM000684.1:g.50928241C>A GRCh37
NC_000022.9:g.49275107C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.814C>A MANE Select ENSP00000216075.6:p.Gln272Lys
ENST00000216075.10:c.814C>A ENSP00000216075.6:p.Gln272Lys
ENST00000395732.7:c.800C>A ENSP00000379081.3:p.Pro267Gln
ENST00000395733.7:c.683C>A ENSP00000379082.3:p.Pro228Gln
ENST00000451761.1:c.754C>A ENSP00000409894.1:p.Gln252Lys
NM_017584.5:c.814C>A NP_060054.4:p.Gln272Lys
XM_005261925.3:c.676C>A XP_005261982.1:p.Gln226Lys
XR_244455.2:n.3310C>A
XM_005261925.4:c.676C>A XP_005261982.1:p.Gln226Lys
NM_017584.6:c.814C>A MANE Select NP_060054.4:p.Gln272Lys