Canonical Allele Identifier: CA2237553667
Gene: MPHOSPH6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82148504A= , CM000678.2:g.82148504A= GRCh38
NC_000016.9:g.82182109A= , CM000678.1:g.82182109A= GRCh37
NC_000016.8:g.80739610A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258169.9:c.*227T= MANE Select ENSP00000258169.4:n.*227T=
ENST00000258169.8:c.*227T= ENSP00000258169.4:n.*227T=
ENST00000563100.5:c.*72+155T= ENSP00000454996.1:n.*72+155T=
NM_005792.2:c.*227T= MANE Select NP_005783.2:n.*227T=
XM_011522808.1:c.*227T= XP_011521110.1:n.*227T=
XM_011522808.3:c.*227T= XP_011521110.1:n.*227T=
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