Canonical Allele Identifier: CA2634540091
Gene: MPHOSPH6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82148517G>A , CM000678.2:g.82148517G>A GRCh38
NC_000016.9:g.82182122G>A , CM000678.1:g.82182122G>A GRCh37
NC_000016.8:g.80739623G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258169.9:c.*214C>T MANE Select ENSP00000258169.4:n.*214C>T
ENST00000258169.8:c.*214C>T ENSP00000258169.4:n.*214C>T
ENST00000563100.5:c.*72+142C>T ENSP00000454996.1:n.*72+142C>T
NM_005792.2:c.*214C>T MANE Select NP_005783.2:n.*214C>T
XM_011522808.1:c.*214C>T XP_011521110.1:n.*214C>T
XM_011522808.3:c.*214C>T XP_011521110.1:n.*214C>T