Canonical Allele Identifier: CA407183397

Gene: PPP2R1A

Linked Data

• MyVariant Identifiers: chr19:g.52715949A>G (hg19) ; chr19:g.52212696A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52212696A>G , CM000681.2:g.52212696A>G	GRCh38
NC_000019.9:g.52715949A>G , CM000681.1:g.52715949A>G	GRCh37
NC_000019.8:g.57407761A>G	NCBI36
NG_047068.1:g.27895A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.634A>G	ENSP00000391905.3:p.Asn212Asp
ENST00000703395.1:c.-24A>G	ENSP00000515286.1:n.-24A>G
ENST00000703396.1:n.458A>G
ENST00000703397.1:c.-24A>G	ENSP00000515287.1:n.-24A>G
ENST00000703398.1:c.556A>G	ENSP00000515288.1:p.Asn186Asp
ENST00000703421.1:n.667A>G
ENST00000703422.1:c.490A>G	ENSP00000515292.1:p.Asn164Asp
ENST00000703423.1:c.-24A>G	ENSP00000515293.1:n.-24A>G
ENST00000322088.11:c.514A>G MANE Select	ENSP00000324804.6:p.Asn172Asp
ENST00000322088.10:c.514A>G	ENSP00000324804.6:p.Asn172Asp
ENST00000454220.6:c.634A>G	ENSP00000391905.2:p.Asn212Asp
ENST00000462047.1:n.205A>G
ENST00000462990.5:c.-24A>G	ENSP00000470504.1:n.-24A>G
ENST00000473455.2:n.613A>G
NM_014225.5:c.514A>G	NP_055040.2:p.Asn172Asp
NR_033500.1:n.708A>G
NM_001363656.1:c.-24A>G	NP_001350585.1:n.-24A>G
NM_014225.6:c.514A>G MANE Select	NP_055040.2:p.Asn172Asp
NM_001363656.2:c.-24A>G	NP_001350585.1:n.-24A>G
NR_033500.2:n.458A>G