Canonical Allele Identifier: CA3024327

Gene: PPP3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101061067C>A , CM000666.2:g.101061067C>A	GRCh38
NC_000004.11:g.101982224C>A , CM000666.1:g.101982224C>A	GRCh37
NC_000004.10:g.102201247C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000944.5:c.1156+20G>T MANE Select	NP_000935.1:n.1156+20G>T
ENST00000394854.8:c.1156+20G>T MANE Select	ENSP00000378323.3:n.1156+20G>T
NM_000944.4:c.1156+20G>T	NP_000935.1:n.1156+20G>T
NM_001130691.1:c.1156+20G>T	NP_001124163.1:n.1156+20G>T
NM_001130691.2:c.1156+20G>T	NP_001124163.1:n.1156+20G>T
NM_001130692.1:c.1030+20G>T	NP_001124164.1:n.1030+20G>T
NM_001130692.2:c.1030+20G>T	NP_001124164.1:n.1030+20G>T
ENST00000323055.10:c.1030+20G>T	ENSP00000320580.6:n.1030+20G>T
ENST00000394853.8:c.1156+20G>T	ENSP00000378322.4:n.1156+20G>T
ENST00000394854.7:c.1156+20G>T	ENSP00000378323.3:n.1156+20G>T
ENST00000507176.5:c.862+20G>T	ENSP00000422990.1:n.862+20G>T
ENST00000512215.5:c.460+20G>T	ENSP00000422781.1:n.460+20G>T
XM_017008365.1:c.1120+20G>T	XP_016863854.1:n.1120+20G>T
XM_024454127.1:c.1006+20G>T	XP_024309895.1:n.1006+20G>T