Canonical Allele Identifier: CA2410885384
Gene: MIOX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50489887_50489913delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG , CM000684.2:g.50489887_50489913delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG GRCh38
NC_000022.10:g.50928316_50928342delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG , CM000684.1:g.50928316_50928342delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG GRCh37
NC_000022.9:g.49275182_49275208delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000216075.11:c.*31_*57delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG MANE Select ENSP00000216075.6:n.*31_*57delinsTAGGCCTG...
ENST00000216075.10:c.*31_*57delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG ENSP00000216075.6:n.*31_*57delinsTAGGCCTG...
ENST00000395732.7:c.*62_*88delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG ENSP00000379081.3:n.*62_*88delinsTAGGCCTG...
ENST00000395733.7:c.*62_*88delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG ENSP00000379082.3:n.*62_*88delinsTAGGCCTG...
ENST00000451761.1:c.829_855delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG ENSP00000409894.1:n.829_855delinsTAGGCCTG...
NM_017584.5:c.*31_*57delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG NP_060054.4:n.*31_*57delinsTAGGCCTGGCCCTC...
XM_005261925.3:c.*31_*57delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG XP_005261982.1:n.*31_*57delinsTAGGCCTGGCC...
XR_244455.2:n.3385_3411delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG
XM_005261925.4:c.*31_*57delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG XP_005261982.1:n.*31_*57delinsTAGGCCTGGCC...
NM_017584.6:c.*31_*57delinsTAGGCCTGGCCCTCCGCCTGCCTGGAG MANE Select NP_060054.4:n.*31_*57delinsTAGGCCTGGCCCTC...