Canonical Allele Identifier: CA16194745

Gene: PPP3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101029379A>C , CM000666.2:g.101029379A>C	GRCh38
NC_000004.11:g.101950536A>C , CM000666.1:g.101950536A>C	GRCh37
NC_000004.10:g.102169559A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000944.5:c.1340-184T>G MANE Select	NP_000935.1:n.1340-184T>G
ENST00000394854.8:c.1340-184T>G MANE Select	ENSP00000378323.3:n.1340-184T>G
NM_000944.4:c.1340-184T>G	NP_000935.1:n.1340-184T>G
NM_001130691.1:c.1339+2888T>G	NP_001124163.1:n.1339+2888T>G
NM_001130691.2:c.1339+2888T>G	NP_001124163.1:n.1339+2888T>G
NM_001130692.1:c.1213+2888T>G	NP_001124164.1:n.1213+2888T>G
NM_001130692.2:c.1213+2888T>G	NP_001124164.1:n.1213+2888T>G
ENST00000323055.10:c.1213+2888T>G	ENSP00000320580.6:n.1213+2888T>G
ENST00000394853.8:c.1339+2888T>G	ENSP00000378322.4:n.1339+2888T>G
ENST00000394854.7:c.1340-184T>G	ENSP00000378323.3:n.1340-184T>G
ENST00000507176.5:c.1046-184T>G	ENSP00000422990.1:n.1046-184T>G
ENST00000512215.5:c.644-184T>G	ENSP00000422781.1:n.644-184T>G
XM_017008365.1:c.1304-184T>G	XP_016863854.1:n.1304-184T>G
XM_024454127.1:c.1190-184T>G	XP_024309895.1:n.1190-184T>G