Canonical Allele Identifier: CA2237553696
Gene: MPHOSPH6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.82148515_82148517delinsAGG , CM000678.2:g.82148515_82148517delinsAGG GRCh38
NC_000016.9:g.82182120_82182122delinsAGG , CM000678.1:g.82182120_82182122delinsAGG GRCh37
NC_000016.8:g.80739621_80739623delinsAGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000258169.9:c.*214_*216delinsCCT MANE Select ENSP00000258169.4:n.*214_*216delinsCCT
ENST00000258169.8:c.*214_*216delinsCCT ENSP00000258169.4:n.*214_*216delinsCCT
ENST00000563100.5:c.*72+142_*72+144delinsCCT ENSP00000454996.1:n.*72+142_*72+144delinsCCT
NM_005792.2:c.*214_*216delinsCCT MANE Select NP_005783.2:n.*214_*216delinsCCT
XM_011522808.1:c.*214_*216delinsCCT XP_011521110.1:n.*214_*216delinsCCT
XM_011522808.3:c.*214_*216delinsCCT XP_011521110.1:n.*214_*216delinsCCT