Canonical Allele Identifier: CA1624305026
Gene: PPP2R5D HGNC NCBI
MEA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43007201A= , CM000668.2:g.43007201A= GRCh38
NC_000006.11:g.42974939A= , CM000668.1:g.42974939A= GRCh37
NC_000006.10:g.43082917A= NCBI36
NG_050636.1:g.27703A=

Transcript Alleles

HGVS Amino-acid change
ENST00000485511.6:c.528A= (PPP2R5D) MANE Select ENSP00000417963.1:p.Ser176=
ENST00000676174.1:n.187A= (PPP2R5D)
ENST00000230402.10:c.*209A= (PPP2R5D) ENSP00000230402.6:n.*209A=
ENST00000394110.7:c.432A= (PPP2R5D) ENSP00000377669.3:p.Ser144=
ENST00000461010.5:c.210A= (PPP2R5D) ENSP00000420674.1:p.Ser70=
ENST00000467447.1:n.105A= (PPP2R5D)
ENST00000470467.5:c.286A= (PPP2R5D)
ENST00000472118.5:c.504A= (PPP2R5D) ENSP00000420550.1:p.Ser168=
ENST00000485511.5:c.528A= (PPP2R5D) ENSP00000417963.1:p.Ser176=
NM_001270476.1:c.75A= (PPP2R5D) NP_001257405.1:p.Ser25=
NM_006245.3:c.528A= (PPP2R5D) NP_006236.1:p.Ser176=
NM_180976.2:c.432A= (PPP2R5D) NP_851307.1:p.Ser144=
NM_180977.2:c.210A= (PPP2R5D) NP_851308.1:p.Ser70=
XM_005249123.1:c.367+5725T= (MEA1) XP_005249180.1:n.367+5725T=
XM_017010868.1:c.367+5725T= (MEA1) XP_016866357.1:n.367+5725T=
NM_006245.4:c.528A= (PPP2R5D) MANE Select NP_006236.1:p.Ser176=
NM_001270476.2:c.75A= (PPP2R5D) NP_001257405.1:p.Ser25=
NM_180976.3:c.432A= (PPP2R5D) NP_851307.1:p.Ser144=
NM_180977.3:c.210A= (PPP2R5D) NP_851308.1:p.Ser70=