Canonical Allele Identifier: CA357947758
Gene: PPP3CA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.101026020C>T , CM000666.2:g.101026020C>T GRCh38
NC_000004.11:g.101947177C>T , CM000666.1:g.101947177C>T GRCh37
NC_000004.10:g.102166200C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394854.8:c.1411G>A MANE Select ENSP00000378323.3:p.Glu471Lys
ENST00000323055.10:c.1255G>A ENSP00000320580.6:p.Glu419Lys
ENST00000394853.8:c.1381G>A ENSP00000378322.4:p.Glu461Lys
ENST00000394854.7:c.1411G>A ENSP00000378323.3:p.Glu471Lys
ENST00000507176.5:c.1117G>A ENSP00000422990.1:p.Glu373Lys
ENST00000512215.5:c.715G>A ENSP00000422781.1:p.Glu239Lys
NM_000944.4:c.1411G>A NP_000935.1:p.Glu471Lys
NM_001130691.1:c.1381G>A NP_001124163.1:p.Glu461Lys
NM_001130692.1:c.1255G>A NP_001124164.1:p.Glu419Lys
XM_017008365.1:c.1375G>A XP_016863854.1:p.Glu459Lys
XM_024454127.1:c.1261G>A XP_024309895.1:p.Glu421Lys
NM_000944.5:c.1411G>A MANE Select NP_000935.1:p.Glu471Lys
NM_001130691.2:c.1381G>A NP_001124163.1:p.Glu461Lys
NM_001130692.2:c.1255G>A NP_001124164.1:p.Glu419Lys