Canonical Allele Identifier: CA357949130

Gene: PPP3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101093803G>C , CM000666.2:g.101093803G>C	GRCh38
NC_000004.11:g.102014960G>C , CM000666.1:g.102014960G>C	GRCh37
NC_000004.10:g.102233983G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394854.8:c.755C>G MANE Select	ENSP00000378323.3:p.Thr252Arg
ENST00000323055.10:c.755C>G	ENSP00000320580.6:p.Thr252Arg
ENST00000394853.8:c.755C>G	ENSP00000378322.4:p.Thr252Arg
ENST00000394854.7:c.755C>G	ENSP00000378323.3:p.Thr252Arg
ENST00000492351.6:c.740C>G	ENSP00000426565.1:n.740C>G
ENST00000507176.5:c.461C>G	ENSP00000422990.1:p.Thr154Arg
ENST00000512215.5:c.260-30446C>G	ENSP00000422781.1:n.260-30446C>G
NM_000944.4:c.755C>G	NP_000935.1:p.Thr252Arg
NM_001130691.1:c.755C>G	NP_001124163.1:p.Thr252Arg
NM_001130692.1:c.755C>G	NP_001124164.1:p.Thr252Arg
XM_017008365.1:c.719C>G	XP_016863854.1:p.Thr240Arg
XM_024454127.1:c.605C>G	XP_024309895.1:p.Thr202Arg
NM_000944.5:c.755C>G MANE Select	NP_000935.1:p.Thr252Arg
NM_001130691.2:c.755C>G	NP_001124163.1:p.Thr252Arg
NM_001130692.2:c.755C>G	NP_001124164.1:p.Thr252Arg