Canonical Allele Identifier: CA2830537531

Gene: PPP3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101109145_101109148del , CM000666.2:g.101109145_101109148del	GRCh38
NC_000004.11:g.102030302_102030305del , CM000666.1:g.102030302_102030305del	GRCh37
NC_000004.10:g.102249325_102249328del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394854.8:c.260-69_260-66del MANE Select	ENSP00000378323.3:n.260-69_260-66del
ENST00000323055.10:c.260-69_260-66del	ENSP00000320580.6:n.260-69_260-66del
ENST00000394853.8:c.260-69_260-66del	ENSP00000378322.4:n.260-69_260-66del
ENST00000394854.7:c.260-69_260-66del	ENSP00000378323.3:n.260-69_260-66del
ENST00000492351.6:c.157-69_157-66del	ENSP00000426565.1:n.157-69_157-66del
ENST00000507176.5:c.-35-69_-35-66del	ENSP00000422990.1:n.-35-69_-35-66del
ENST00000510292.1:n.151-69_151-66del
ENST00000512215.5:c.260-45790_260-45787del	ENSP00000422781.1:n.260-45790_260-45787del
ENST00000525819.1:c.110-69_110-66del	ENSP00000434599.1:n.110-69_110-66del
ENST00000529324.5:c.110-69_110-66del	ENSP00000431619.1:n.110-69_110-66del
NM_000944.4:c.260-69_260-66del	NP_000935.1:n.260-69_260-66del
NM_001130691.1:c.260-69_260-66del	NP_001124163.1:n.260-69_260-66del
NM_001130692.1:c.260-69_260-66del	NP_001124164.1:n.260-69_260-66del
XM_017008365.1:c.224-69_224-66del	XP_016863854.1:n.224-69_224-66del
XM_024454127.1:c.110-69_110-66del	XP_024309895.1:n.110-69_110-66del
NM_000944.5:c.260-69_260-66del MANE Select	NP_000935.1:n.260-69_260-66del
NM_001130691.2:c.260-69_260-66del	NP_001124163.1:n.260-69_260-66del
NM_001130692.2:c.260-69_260-66del	NP_001124164.1:n.260-69_260-66del