Canonical Allele Identifier: CA2237553569
Gene: MPHOSPH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82148450A= , CM000678.2:g.82148450A= GRCh38
NC_000016.9:g.82182055A= , CM000678.1:g.82182055A= GRCh37
NC_000016.8:g.80739556A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258169.9:c.*281T= MANE Select ENSP00000258169.4:n.*281T=
ENST00000258169.8:c.*281T= ENSP00000258169.4:n.*281T=
ENST00000563100.5:c.*72+209T= ENSP00000454996.1:n.*72+209T=
NM_005792.2:c.*281T= MANE Select NP_005783.2:n.*281T=
XM_011522808.1:c.*281T= XP_011521110.1:n.*281T=
XM_011522808.3:c.*281T= XP_011521110.1:n.*281T=