Canonical Allele Identifier: CA3024502

Gene: PPP3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101099767C>T , CM000666.2:g.101099767C>T	GRCh38
NC_000004.11:g.102020924C>T , CM000666.1:g.102020924C>T	GRCh37
NC_000004.10:g.102239947C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000944.5:c.385-45G>A MANE Select	NP_000935.1:n.385-45G>A
ENST00000394854.8:c.385-45G>A MANE Select	ENSP00000378323.3:n.385-45G>A
NM_000944.4:c.385-45G>A	NP_000935.1:n.385-45G>A
NM_001130691.1:c.385-45G>A	NP_001124163.1:n.385-45G>A
NM_001130691.2:c.385-45G>A	NP_001124163.1:n.385-45G>A
NM_001130692.1:c.385-45G>A	NP_001124164.1:n.385-45G>A
NM_001130692.2:c.385-45G>A	NP_001124164.1:n.385-45G>A
ENST00000323055.10:c.385-45G>A	ENSP00000320580.6:n.385-45G>A
ENST00000394853.8:c.385-45G>A	ENSP00000378322.4:n.385-45G>A
ENST00000394854.7:c.385-45G>A	ENSP00000378323.3:n.385-45G>A
ENST00000492351.6:c.370-45G>A	ENSP00000426565.1:n.370-45G>A
ENST00000507176.5:c.91-45G>A	ENSP00000422990.1:n.91-45G>A
ENST00000510292.1:n.276-45G>A
ENST00000512215.5:c.260-36410G>A	ENSP00000422781.1:n.260-36410G>A
ENST00000525819.1:c.235-45G>A	ENSP00000434599.1:n.235-45G>A
ENST00000529324.5:c.235-45G>A	ENSP00000431619.1:n.235-45G>A
XM_017008365.1:c.349-45G>A	XP_016863854.1:n.349-45G>A
XM_024454127.1:c.235-45G>A	XP_024309895.1:n.235-45G>A