Canonical Allele Identifier: CA224150145

Gene: PPP1CA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.67401088T>C , CM000673.2:g.67401088T>C	GRCh38
NC_000011.9:g.67168559T>C , CM000673.1:g.67168559T>C	GRCh37
NC_000011.8:g.66925135T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002708.4:c.167A>G MANE Select	NP_002699.1:p.Glu56Gly
ENST00000376745.9:c.167A>G MANE Select	ENSP00000365936.4:p.Glu56Gly
NM_001008709.1:c.200A>G	NP_001008709.1:p.Glu67Gly
NM_001008709.2:c.200A>G	NP_001008709.1:p.Glu67Gly
NM_002708.3:c.167A>G	NP_002699.1:p.Glu56Gly
NM_206873.1:c.56-169A>G	NP_996756.1:n.56-169A>G
NM_206873.2:c.56-169A>G	NP_996756.1:n.56-169A>G
ENST00000312989.11:c.200A>G	ENSP00000326031.7:p.Glu67Gly
ENST00000358239.8:c.56-169A>G	ENSP00000350974.4:n.56-169A>G
ENST00000376745.8:c.167A>G	ENSP00000365936.4:p.Glu56Gly
ENST00000526510.5:n.517A>G
ENST00000526510.6:n.248A>G
ENST00000527663.5:c.167A>G	ENSP00000431146.1:p.Glu56Gly
ENST00000527663.6:c.167A>G	ENSP00000431146.2:p.Glu56Gly
ENST00000529724.1:n.200A>G
ENST00000532279.2:n.248A>G
ENST00000532446.5:n.305A>G
ENST00000537694.1:n.298A>G
ENST00000537694.2:n.298A>G
ENST00000542876.1:c.458A>G	ENSP00000438409.1:p.Glu153Gly
ENST00000546202.5:c.422A>G	ENSP00000439568.1:p.Glu141Gly
ENST00000677322.1:n.248A>G
ENST00000677343.1:n.248A>G
ENST00000679175.1:c.182A>G	ENSP00000503926.1:p.Glu61Gly