Canonical Allele Identifier: CA407184110
Gene: PPP2R1A HGNC NCBI

Linked Data

dbSNP Id: rs1284984038

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52212823C>T , CM000681.2:g.52212823C>T GRCh38
NC_000019.9:g.52716076C>T , CM000681.1:g.52716076C>T GRCh37
NC_000019.8:g.57407888C>T NCBI36
NG_047068.1:g.28022C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000454220.7:c.761C>T ENSP00000391905.3:p.Ser254Phe
ENST00000703395.1:c.104C>T ENSP00000515286.1:p.Ser35Phe
ENST00000703396.1:n.585C>T
ENST00000703397.1:c.104C>T ENSP00000515287.1:p.Ser35Phe
ENST00000703398.1:c.683C>T ENSP00000515288.1:p.Ser228Phe
ENST00000703421.1:n.794C>T
ENST00000703422.1:c.617C>T ENSP00000515292.1:p.Ser206Phe
ENST00000703423.1:c.104C>T ENSP00000515293.1:p.Ser35Phe
ENST00000322088.11:c.641C>T MANE Select ENSP00000324804.6:p.Ser214Phe
ENST00000322088.10:c.641C>T ENSP00000324804.6:p.Ser214Phe
ENST00000454220.6:c.761C>T ENSP00000391905.2:p.Ser254Phe
ENST00000462047.1:n.332C>T
ENST00000462990.5:c.104C>T ENSP00000470504.1:p.Ser35Phe
NM_014225.5:c.641C>T NP_055040.2:p.Ser214Phe
NR_033500.1:n.835C>T
NM_001363656.1:c.104C>T NP_001350585.1:p.Ser35Phe
NM_014225.6:c.641C>T MANE Select NP_055040.2:p.Ser214Phe
NM_001363656.2:c.104C>T NP_001350585.1:p.Ser35Phe
NR_033500.2:n.585C>T