Canonical Allele Identifier: CA3412934

Gene: PPP2CA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134225898G>C , CM000667.2:g.134225898G>C	GRCh38
NC_000005.9:g.133561589G>C , CM000667.1:g.133561589G>C	GRCh37
NC_000005.8:g.133589488G>C	NCBI36
NG_046997.1:g.5362C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_002715.4:c.-37C>G MANE Select	NP_002706.1:n.-37C>G
ENST00000481195.6:c.-37C>G MANE Select	ENSP00000418447.1:n.-37C>G
NM_002715.2:c.-37C>G	NP_002706.1:n.-37C>G
NM_002715.3:c.-37C>G	NP_002706.1:n.-37C>G
ENST00000231504.5:n.176C>G
ENST00000481195.5:c.-37C>G	ENSP00000418447.1:n.-37C>G
ENST00000518409.2:n.905-19767C>G
ENST00000519718.1:c.-37C>G	ENSP00000430774.1:n.-37C>G
ENST00000520515.5:n.1227-19767C>G
ENST00000703308.1:c.-37C>G	ENSP00000515254.1:n.-37C>G
ENST00000703309.1:c.-37C>G	ENSP00000515255.1:n.-37C>G
ENST00000703312.1:n.430-19767C>G
ENST00000703313.1:c.*635-19767C>G	ENSP00000515258.1:n.*635-19767C>G
ENST00000703316.1:n.890-19767C>G
ENST00000703317.1:c.*73+16994C>G	ENSP00000515260.1:n.*73+16994C>G
ENST00000703354.1:c.-37C>G	ENSP00000515268.1:n.-37C>G
ENST00000703355.1:n.1217+5143C>G