Canonical Allele Identifier: CA364172508

Gene: PPP2R5D MEA1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.42984685A>T , CM000668.2:g.42984685A>T	GRCh38
NC_000006.11:g.42952423A>T , CM000668.1:g.42952423A>T	GRCh37
NC_000006.10:g.43060401A>T	NCBI36
NG_050636.1:g.5187A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_006245.4:c.8A>T (PPP2R5D) MANE Select	NP_006236.1:p.Tyr3Phe
ENST00000485511.6:c.8A>T (PPP2R5D) MANE Select	ENSP00000417963.1:p.Tyr3Phe
NM_001270476.1:c.-463A>T (PPP2R5D)	NP_001257405.1:n.-463A>T
NM_001270476.2:c.-463A>T (PPP2R5D)	NP_001257405.1:n.-463A>T
NM_006245.3:c.8A>T (PPP2R5D)	NP_006236.1:p.Tyr3Phe
NM_180976.2:c.8A>T (PPP2R5D)	NP_851307.1:p.Tyr3Phe
NM_180976.3:c.8A>T (PPP2R5D)	NP_851307.1:p.Tyr3Phe
NM_180977.2:c.8A>T (PPP2R5D)	NP_851308.1:p.Tyr3Phe
NM_180977.3:c.8A>T (PPP2R5D)	NP_851308.1:p.Tyr3Phe
ENST00000230402.10:c.8A>T (PPP2R5D)	ENSP00000230402.6:p.Tyr3Phe
ENST00000394110.7:c.8A>T (PPP2R5D)	ENSP00000377669.3:p.Tyr3Phe
ENST00000461010.5:c.8A>T (PPP2R5D)	ENSP00000420674.1:p.Tyr3Phe
ENST00000472118.5:c.8A>T (PPP2R5D)	ENSP00000420550.1:p.Tyr3Phe
ENST00000485511.5:c.8A>T (PPP2R5D)	ENSP00000417963.1:p.Tyr3Phe
XM_005249123.1:c.368-3842T>A (MEA1)	XP_005249180.1:n.368-3842T>A
XM_017010868.1:c.368-3842T>A (MEA1)	XP_016866357.1:n.368-3842T>A