Canonical Allele Identifier: CA309851913

Gene: PPP2R1A

Linked Data

• dbSNP Id: rs111995435
• MyVariant Identifiers: chr19:g.52693428G>C (hg19) ; chr19:g.52190175G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.52190175G>C , CM000681.2:g.52190175G>C	GRCh38
NC_000019.9:g.52693428G>C , CM000681.1:g.52693428G>C	GRCh37
NC_000019.8:g.57385240G>C	NCBI36
NG_047068.1:g.5374G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000454220.7:c.79G>C	ENSP00000391905.3:p.Val27Leu
ENST00000703395.1:c.-459-11769G>C	ENSP00000515286.1:n.-459-11769G>C
ENST00000703396.1:n.123+1G>C
ENST00000703397.1:c.-657+1G>C	ENSP00000515287.1:n.-657+1G>C
ENST00000703398.1:c.78+1G>C	ENSP00000515288.1:n.78+1G>C
ENST00000703421.1:n.231+1019G>C
ENST00000703422.1:c.78+1G>C	ENSP00000515292.1:n.78+1G>C
ENST00000322088.11:c.78+1G>C MANE Select	ENSP00000324804.6:n.78+1G>C
ENST00000322088.10:c.78+1G>C	ENSP00000324804.6:n.78+1G>C
ENST00000454220.6:c.79G>C	ENSP00000391905.2:p.Val27Leu
ENST00000468280.5:n.61+1G>C
ENST00000477989.1:c.78+1G>C	ENSP00000471298.1:n.78+1G>C
ENST00000490868.5:c.78+1G>C	ENSP00000469150.1:n.78+1G>C
ENST00000628959.1:c.78+1G>C	ENSP00000485914.1:n.78+1G>C
NM_014225.5:c.78+1G>C	NP_055040.2:n.78+1G>C
NR_033500.1:n.373+1G>C
NM_014225.6:c.78+1G>C MANE Select	NP_055040.2:n.78+1G>C
NR_033500.2:n.123+1G>C