Canonical Allele Identifier: CA9621256
Community Standard Title: NM_014225.6(PPP2R1A):c.79-16C>T
Gene: PPP2R1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.52201928C>T , CM000681.2:g.52201928C>T GRCh38
NC_000019.9:g.52705181C>T , CM000681.1:g.52705181C>T GRCh37
NC_000019.8:g.57396993C>T NCBI36
NG_047068.1:g.17127C>T

Transcript Alleles

HGVS Amino-acid Change
NM_014225.6:c.79-16C>T MANE Select NP_055040.2:n.79-16C>T
ENST00000322088.11:c.79-16C>T MANE Select ENSP00000324804.6:n.79-16C>T
NM_001363656.1:c.-459-16C>T NP_001350585.1:n.-459-16C>T
NM_001363656.2:c.-459-16C>T NP_001350585.1:n.-459-16C>T
NM_014225.5:c.79-16C>T NP_055040.2:n.79-16C>T
NR_033500.1:n.374-16C>T
NR_033500.2:n.124-16C>T
ENST00000322088.10:c.79-16C>T ENSP00000324804.6:n.79-16C>T
ENST00000454220.6:c.199-16C>T ENSP00000391905.2:n.199-16C>T
ENST00000454220.7:c.199-16C>T ENSP00000391905.3:n.199-16C>T
ENST00000462990.5:c.-459-16C>T ENSP00000470504.1:n.-459-16C>T
ENST00000468280.5:n.62-16C>T
ENST00000473455.2:n.162C>T
ENST00000490868.5:c.*87-16C>T ENSP00000469150.1:n.*87-16C>T
ENST00000495876.5:n.334-16C>T
ENST00000703395.1:c.-459-16C>T ENSP00000515286.1:n.-459-16C>T
ENST00000703396.1:n.124-16C>T
ENST00000703397.1:c.-459-16C>T ENSP00000515287.1:n.-459-16C>T
ENST00000703398.1:c.79-16C>T ENSP00000515288.1:n.79-16C>T
ENST00000703399.1:n.457-16C>T
ENST00000703421.1:n.232-16C>T
ENST00000703422.1:c.79-16C>T ENSP00000515292.1:n.79-16C>T
ENST00000703423.1:c.-459-16C>T ENSP00000515293.1:n.-459-16C>T