Canonical Allele Identifier: CA11944172

Gene: PPP2CA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134216763C>T , CM000667.2:g.134216763C>T	GRCh38
NC_000005.9:g.133552454C>T , CM000667.1:g.133552454C>T	GRCh37
NC_000005.8:g.133580353C>T	NCBI36
NG_046997.1:g.14497G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002715.4:c.102+8997G>A MANE Select	NP_002706.1:n.102+8997G>A
ENST00000481195.6:c.102+8997G>A MANE Select	ENSP00000418447.1:n.102+8997G>A
NM_001355019.1:c.-94+8446G>A	NP_001341948.1:n.-94+8446G>A
NM_001355019.2:c.-94+8446G>A	NP_001341948.1:n.-94+8446G>A
NM_002715.2:c.102+8997G>A	NP_002706.1:n.102+8997G>A
NM_002715.3:c.102+8997G>A	NP_002706.1:n.102+8997G>A
NR_149151.1:n.346+8446G>A
NR_149151.2:n.346+8446G>A
ENST00000231504.5:n.314+8997G>A
ENST00000481195.5:c.102+8997G>A	ENSP00000418447.1:n.102+8997G>A
ENST00000518409.2:n.905-10632G>A
ENST00000519718.1:c.102+8997G>A	ENSP00000430774.1:n.102+8997G>A
ENST00000519718.2:c.102+8997G>A	ENSP00000430774.2:n.102+8997G>A
ENST00000520515.5:n.1227-10632G>A
ENST00000522385.1:c.-94+8678G>A	ENSP00000430869.1:n.-94+8678G>A
ENST00000522385.2:c.-94+8678G>A	ENSP00000430869.2:n.-94+8678G>A
ENST00000523082.1:c.63+7494G>A	ENSP00000428816.1:n.63+7494G>A
ENST00000703308.1:c.102+8997G>A	ENSP00000515254.1:n.102+8997G>A
ENST00000703309.1:c.102+8997G>A	ENSP00000515255.1:n.102+8997G>A
ENST00000703310.1:c.-94+8446G>A	ENSP00000515256.1:n.-94+8446G>A
ENST00000703311.1:c.-94+8446G>A	ENSP00000515257.1:n.-94+8446G>A
ENST00000703312.1:n.430-10632G>A
ENST00000703313.1:c.*635-10632G>A	ENSP00000515258.1:n.*635-10632G>A
ENST00000703316.1:n.890-10632G>A
ENST00000703317.1:c.*74-10632G>A	ENSP00000515260.1:n.*74-10632G>A
ENST00000703354.1:c.102+8997G>A	ENSP00000515268.1:n.102+8997G>A
ENST00000703355.1:n.1218-10632G>A