Canonical Allele Identifier: CA357948334

Gene: PPP3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101040552C>A , CM000666.2:g.101040552C>A	GRCh38
NC_000004.11:g.101961709C>A , CM000666.1:g.101961709C>A	GRCh37
NC_000004.10:g.102180732C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000944.5:c.1171G>T MANE Select	NP_000935.1:p.Ala391Ser
ENST00000394854.8:c.1171G>T MANE Select	ENSP00000378323.3:p.Ala391Ser
NM_000944.4:c.1171G>T	NP_000935.1:p.Ala391Ser
NM_001130691.1:c.1171G>T	NP_001124163.1:p.Ala391Ser
NM_001130691.2:c.1171G>T	NP_001124163.1:p.Ala391Ser
NM_001130692.1:c.1045G>T	NP_001124164.1:p.Ala349Ser
NM_001130692.2:c.1045G>T	NP_001124164.1:p.Ala349Ser
ENST00000323055.10:c.1045G>T	ENSP00000320580.6:p.Ala349Ser
ENST00000394853.8:c.1171G>T	ENSP00000378322.4:p.Ala391Ser
ENST00000394854.7:c.1171G>T	ENSP00000378323.3:p.Ala391Ser
ENST00000507176.5:c.877G>T	ENSP00000422990.1:p.Ala293Ser
ENST00000512215.5:c.475G>T	ENSP00000422781.1:p.Ala159Ser
XM_017008365.1:c.1135G>T	XP_016863854.1:p.Ala379Ser
XM_024454127.1:c.1021G>T	XP_024309895.1:p.Ala341Ser