Canonical Allele Identifier: CA11853075

Gene: PPP3CA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.101025791T>C , CM000666.2:g.101025791T>C	GRCh38
NC_000004.11:g.101946948T>C , CM000666.1:g.101946948T>C	GRCh37
NC_000004.10:g.102165971T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_000944.5:c.*74A>G MANE Select	NP_000935.1:n.*74A>G
ENST00000394854.8:c.*74A>G MANE Select	ENSP00000378323.3:n.*74A>G
NM_000944.4:c.*74A>G	NP_000935.1:n.*74A>G
NM_001130691.1:c.*74A>G	NP_001124163.1:n.*74A>G
NM_001130691.2:c.*74A>G	NP_001124163.1:n.*74A>G
NM_001130692.1:c.*74A>G	NP_001124164.1:n.*74A>G
NM_001130692.2:c.*74A>G	NP_001124164.1:n.*74A>G
ENST00000323055.10:c.*74A>G	ENSP00000320580.6:n.*74A>G
ENST00000394853.8:c.*74A>G	ENSP00000378322.4:n.*74A>G
ENST00000394854.7:c.*74A>G	ENSP00000378323.3:n.*74A>G
ENST00000507176.5:c.*74A>G	ENSP00000422990.1:n.*74A>G
ENST00000512215.5:c.*74A>G	ENSP00000422781.1:n.*74A>G
XM_017008365.1:c.*74A>G	XP_016863854.1:n.*74A>G
XM_024454127.1:c.*74A>G	XP_024309895.1:n.*74A>G