Canonical Allele Identifier: CA1480765861

Gene: PPP3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101126867G= , CM000666.2:g.101126867G=	GRCh38
NC_000004.11:g.102048024G= , CM000666.1:g.102048024G=	GRCh37
NC_000004.10:g.102267047G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394854.8:c.260-17789C= MANE Select	ENSP00000378323.3:n.260-17789C=
ENST00000323055.10:c.260-17789C=	ENSP00000320580.6:n.260-17789C=
ENST00000394853.8:c.260-17789C=	ENSP00000378322.4:n.260-17789C=
ENST00000394854.7:c.260-17789C=	ENSP00000378323.3:n.260-17789C=
ENST00000492351.6:c.157-17789C=	ENSP00000426565.1:n.157-17789C=
ENST00000507176.5:c.-35-17789C=	ENSP00000422990.1:n.-35-17789C=
ENST00000510292.1:n.151-17789C=
ENST00000512215.5:c.260-63510C=	ENSP00000422781.1:n.260-63510C=
ENST00000525819.1:c.110-17789C=	ENSP00000434599.1:n.110-17789C=
ENST00000529324.5:c.110-17789C=	ENSP00000431619.1:n.110-17789C=
NM_000944.4:c.260-17789C=	NP_000935.1:n.260-17789C=
NM_001130691.1:c.260-17789C=	NP_001124163.1:n.260-17789C=
NM_001130692.1:c.260-17789C=	NP_001124164.1:n.260-17789C=
XM_017008365.1:c.224-17789C=	XP_016863854.1:n.224-17789C=
XM_024454127.1:c.110-17789C=	XP_024309895.1:n.110-17789C=
NM_000944.5:c.260-17789C= MANE Select	NP_000935.1:n.260-17789C=
NM_001130691.2:c.260-17789C=	NP_001124163.1:n.260-17789C=
NM_001130692.2:c.260-17789C=	NP_001124164.1:n.260-17789C=