Canonical Allele Identifier: CA979716568
Gene: MPHOSPH6 HGNC NCBI

Linked Data

dbSNP Id: rs1906151627

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82148458C>A , CM000678.2:g.82148458C>A GRCh38
NC_000016.9:g.82182063C>A , CM000678.1:g.82182063C>A GRCh37
NC_000016.8:g.80739564C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258169.9:c.*273G>T MANE Select ENSP00000258169.4:n.*273G>T
ENST00000258169.8:c.*273G>T ENSP00000258169.4:n.*273G>T
ENST00000563100.5:c.*72+201G>T ENSP00000454996.1:n.*72+201G>T
NM_005792.2:c.*273G>T MANE Select NP_005783.2:n.*273G>T
XM_011522808.1:c.*273G>T XP_011521110.1:n.*273G>T
XM_011522808.3:c.*273G>T XP_011521110.1:n.*273G>T