Canonical Allele Identifier: CA2142228823

Gene: PPP2R5E

Linked Data

• dbSNP Id: rs11158493

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.63486804C>G , CM000676.2:g.63486804C>G	GRCh38
NC_000014.8:g.63953522C>G , CM000676.1:g.63953522C>G	GRCh37
NC_000014.7:g.63023275C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000337537.8:c.158-32919G>C MANE Select	ENSP00000337641.3:n.158-32919G>C
ENST00000337537.7:c.158-32919G>C	ENSP00000337641.3:n.158-32919G>C
ENST00000422769.6:c.-72+21321G>C	ENSP00000404632.2:n.-72+21321G>C
ENST00000553266.5:n.740+52725G>C
ENST00000555899.1:c.158-32919G>C	ENSP00000452396.1:n.158-32919G>C
ENST00000556484.5:n.114+21321G>C
ENST00000556878.1:n.760-32919G>C
NM_001282179.1:c.158-32919G>C	NP_001269108.1:n.158-32919G>C
NM_001282180.1:c.158-32919G>C	NP_001269109.1:n.158-32919G>C
NM_001282181.1:c.-72+21321G>C	NP_001269110.1:n.-72+21321G>C
NM_001282182.1:c.-72+21366G>C	NP_001269111.1:n.-72+21366G>C
NM_006246.3:c.158-32919G>C	NP_006237.1:n.158-32919G>C
NR_104104.1:n.747+52725G>C
XM_011536922.1:c.158-32919G>C	XP_011535224.1:n.158-32919G>C
NM_001282179.2:c.158-32919G>C	NP_001269108.1:n.158-32919G>C
NM_001282180.2:c.158-32919G>C	NP_001269109.1:n.158-32919G>C
NM_001282181.2:c.-72+21321G>C	NP_001269110.1:n.-72+21321G>C
NM_001282182.2:c.-72+21366G>C	NP_001269111.1:n.-72+21366G>C
NM_001354926.1:c.158-32919G>C	NP_001341855.1:n.158-32919G>C
NM_006246.4:c.158-32919G>C	NP_006237.1:n.158-32919G>C
NR_104104.2:n.781+52725G>C
XM_024449647.1:c.158-32919G>C	XP_024305415.1:n.158-32919G>C
NM_006246.5:c.158-32919G>C MANE Select	NP_006237.1:n.158-32919G>C
NM_001282179.3:c.158-32919G>C	NP_001269108.1:n.158-32919G>C
NM_001282180.3:c.158-32919G>C	NP_001269109.1:n.158-32919G>C
NM_001282182.3:c.-72+21366G>C	NP_001269111.1:n.-72+21366G>C
NR_104104.3:n.763+52725G>C
NM_001282181.3:c.-72+21321G>C	NP_001269110.1:n.-72+21321G>C
NM_001354926.2:c.158-32919G>C	NP_001341855.1:n.158-32919G>C