Canonical Allele Identifier: CA2634540013
Gene: MPHOSPH6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82148426G>T , CM000678.2:g.82148426G>T GRCh38
NC_000016.9:g.82182031G>T , CM000678.1:g.82182031G>T GRCh37
NC_000016.8:g.80739532G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258169.9:c.*305C>A MANE Select ENSP00000258169.4:n.*305C>A
ENST00000258169.8:c.*305C>A ENSP00000258169.4:n.*305C>A
ENST00000563100.5:c.*72+233C>A ENSP00000454996.1:n.*72+233C>A
NM_005792.2:c.*305C>A MANE Select NP_005783.2:n.*305C>A
XM_011522808.1:c.*305C>A XP_011521110.1:n.*305C>A
XM_011522808.3:c.*305C>A XP_011521110.1:n.*305C>A