Canonical Allele Identifier: CA1374494757

Gene: PPP4R2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.73053574A= , CM000665.2:g.73053574A=	GRCh38
NC_000003.11:g.73102725A= , CM000665.1:g.73102725A=	GRCh37
NC_000003.10:g.73185415A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_174907.4:c.288-5463A= MANE Select	NP_777567.1:n.288-5463A=
ENST00000356692.10:c.288-5463A= MANE Select	ENSP00000349124.5:n.288-5463A=
NM_001318025.1:c.117-5463A=	NP_001304954.1:n.117-5463A=
NM_001318025.2:c.117-5463A=	NP_001304954.1:n.117-5463A=
NM_001318026.1:c.174-5463A=	NP_001304955.1:n.174-5463A=
NM_001318026.2:c.174-5463A=	NP_001304955.1:n.174-5463A=
NM_001318027.1:c.-164-5463A=	NP_001304956.1:n.-164-5463A=
NM_001318027.2:c.-164-5463A=	NP_001304956.1:n.-164-5463A=
NM_174907.2:c.288-5463A=	NP_777567.1:n.288-5463A=
NM_174907.3:c.288-5463A=	NP_777567.1:n.288-5463A=
ENST00000356692.9:c.288-5463A=	ENSP00000349124.5:n.288-5463A=
ENST00000470976.1:n.508-5463A=
ENST00000476505.2:c.174-5463A=	ENSP00000420098.2:n.174-5463A=
ENST00000482242.5:c.117-5463A=	ENSP00000418568.1:n.117-5463A=
ENST00000488810.5:c.288-5463A=	ENSP00000418750.1:n.288-5463A=
ENST00000710398.1:c.393-5463A=	ENSP00000518252.1:n.393-5463A=