Canonical Allele Identifier: CA364181088

Gene: PPP2R5D MEA1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43006649C>G , CM000668.2:g.43006649C>G	GRCh38
NC_000006.11:g.42974387C>G , CM000668.1:g.42974387C>G	GRCh37
NC_000006.10:g.43082365C>G	NCBI36
NG_050636.1:g.27151C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006245.4:c.292C>G (PPP2R5D) MANE Select	NP_006236.1:p.Arg98Gly
ENST00000485511.6:c.292C>G (PPP2R5D) MANE Select	ENSP00000417963.1:p.Arg98Gly
NM_001270476.1:c.-162C>G (PPP2R5D)	NP_001257405.1:n.-162C>G
NM_001270476.2:c.-162C>G (PPP2R5D)	NP_001257405.1:n.-162C>G
NM_006245.3:c.292C>G (PPP2R5D)	NP_006236.1:p.Arg98Gly
NM_180976.2:c.249+43C>G (PPP2R5D)	NP_851307.1:n.249+43C>G
NM_180976.3:c.249+43C>G (PPP2R5D)	NP_851307.1:n.249+43C>G
NM_180977.2:c.28-285C>G (PPP2R5D)	NP_851308.1:n.28-285C>G
NM_180977.3:c.28-285C>G (PPP2R5D)	NP_851308.1:n.28-285C>G
ENST00000230402.10:c.309C>G (PPP2R5D)	ENSP00000230402.6:p.Ile103Met
ENST00000394110.7:c.249+43C>G (PPP2R5D)	ENSP00000377669.3:n.249+43C>G
ENST00000461010.5:c.28-285C>G (PPP2R5D)	ENSP00000420674.1:n.28-285C>G
ENST00000470467.5:c.50C>G (PPP2R5D)
ENST00000472118.5:c.268C>G (PPP2R5D)	ENSP00000420550.1:p.Arg90Gly
ENST00000485511.5:c.292C>G (PPP2R5D)	ENSP00000417963.1:p.Arg98Gly
XM_005249123.1:c.367+6277G>C (MEA1)	XP_005249180.1:n.367+6277G>C
XM_017010868.1:c.367+6277G>C (MEA1)	XP_016866357.1:n.367+6277G>C