Canonical Allele Identifier: CA1702779

Gene: MPHOSPH10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.71132930C>A , CM000664.2:g.71132930C>A	GRCh38
NC_000002.11:g.71360060C>A , CM000664.1:g.71360060C>A	GRCh37
NC_000002.10:g.71213568C>A	NCBI36
NG_008977.1:g.2335G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005791.3:c.122C>A MANE Select	NP_005782.1:p.Ser41Tyr
ENST00000244230.7:c.122C>A MANE Select	ENSP00000244230.2:p.Ser41Tyr
NM_005791.2:c.122C>A	NP_005782.1:p.Ser41Tyr
ENST00000244230.6:c.122C>A	ENSP00000244230.2:p.Ser41Tyr
ENST00000468427.1:n.245C>A
ENST00000468427.2:c.-299C>A	ENSP00000511582.1:n.-299C>A
ENST00000498451.2:c.122C>A	ENSP00000475545.1:p.Ser41Tyr
ENST00000498451.3:c.122C>A	ENSP00000475545.1:p.Ser41Tyr
ENST00000694907.2:c.90-155C>A	ENSP00000511583.1:n.90-155C>A
ENST00000695484.2:c.122C>A	ENSP00000511956.1:p.Ser41Tyr