Canonical Allele Identifier: CA357949790
Gene: PPP3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101080622G>T , CM000666.2:g.101080622G>T GRCh38
NC_000004.11:g.102001779G>T , CM000666.1:g.102001779G>T GRCh37
NC_000004.10:g.102220802G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394854.8:c.865C>A MANE Select ENSP00000378323.3:p.Arg289Ser
ENST00000323055.10:c.865C>A ENSP00000320580.6:p.Arg289Ser
ENST00000394853.8:c.865C>A ENSP00000378322.4:p.Arg289Ser
ENST00000394854.7:c.865C>A ENSP00000378323.3:p.Arg289Ser
ENST00000507176.5:c.571C>A ENSP00000422990.1:p.Arg191Ser
ENST00000512215.5:c.260-17265C>A ENSP00000422781.1:n.260-17265C>A
NM_000944.4:c.865C>A NP_000935.1:p.Arg289Ser
NM_001130691.1:c.865C>A NP_001124163.1:p.Arg289Ser
NM_001130692.1:c.865C>A NP_001124164.1:p.Arg289Ser
XM_017008365.1:c.829C>A XP_016863854.1:p.Arg277Ser
XM_024454127.1:c.715C>A XP_024309895.1:p.Arg239Ser
NM_000944.5:c.865C>A MANE Select NP_000935.1:p.Arg289Ser
NM_001130691.2:c.865C>A NP_001124163.1:p.Arg289Ser
NM_001130692.2:c.865C>A NP_001124164.1:p.Arg289Ser