Canonical Allele Identifier: CA412150566
Gene: MIOX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489823T>C , CM000684.2:g.50489823T>C GRCh38
NC_000022.10:g.50928252T>C , CM000684.1:g.50928252T>C GRCh37
NC_000022.9:g.49275118T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.825T>C MANE Select ENSP00000216075.6:p.Ile275=
ENST00000216075.10:c.825T>C ENSP00000216075.6:p.Ile275=
ENST00000395732.7:c.811T>C ENSP00000379081.3:p.Ter271Arg
ENST00000395733.7:c.694T>C ENSP00000379082.3:p.Ter232Arg
ENST00000451761.1:c.765T>C ENSP00000409894.1:p.Ile255=
NM_017584.5:c.825T>C NP_060054.4:p.Ile275=
XM_005261925.3:c.687T>C XP_005261982.1:p.Ile229=
XR_244455.2:n.3321T>C
XM_005261925.4:c.687T>C XP_005261982.1:p.Ile229=
NM_017584.6:c.825T>C MANE Select NP_060054.4:p.Ile275=