Canonical Allele Identifier: CA364184299

Gene: PPP2R5D MEA1

Linked Data

• MyVariant Identifiers: chr6:g.42974937T>A (hg19) ; chr6:g.43007199T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.43007199T>A , CM000668.2:g.43007199T>A	GRCh38
NC_000006.11:g.42974937T>A , CM000668.1:g.42974937T>A	GRCh37
NC_000006.10:g.43082915T>A	NCBI36
NG_050636.1:g.27701T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000485511.6:c.526T>A (PPP2R5D) MANE Select	ENSP00000417963.1:p.Ser176Thr
ENST00000676174.1:n.185T>A (PPP2R5D)
ENST00000230402.10:c.*207T>A (PPP2R5D)	ENSP00000230402.6:n.*207T>A
ENST00000394110.7:c.430T>A (PPP2R5D)	ENSP00000377669.3:p.Ser144Thr
ENST00000461010.5:c.208T>A (PPP2R5D)	ENSP00000420674.1:p.Ser70Thr
ENST00000467447.1:n.103T>A (PPP2R5D)
ENST00000470467.5:c.284T>A (PPP2R5D)
ENST00000472118.5:c.502T>A (PPP2R5D)	ENSP00000420550.1:p.Ser168Thr
ENST00000485511.5:c.526T>A (PPP2R5D)	ENSP00000417963.1:p.Ser176Thr
NM_001270476.1:c.73T>A (PPP2R5D)	NP_001257405.1:p.Ser25Thr
NM_006245.3:c.526T>A (PPP2R5D)	NP_006236.1:p.Ser176Thr
NM_180976.2:c.430T>A (PPP2R5D)	NP_851307.1:p.Ser144Thr
NM_180977.2:c.208T>A (PPP2R5D)	NP_851308.1:p.Ser70Thr
XM_005249123.1:c.367+5727A>T (MEA1)	XP_005249180.1:n.367+5727A>T
XM_017010868.1:c.367+5727A>T (MEA1)	XP_016866357.1:n.367+5727A>T
NM_006245.4:c.526T>A (PPP2R5D) MANE Select	NP_006236.1:p.Ser176Thr
NM_001270476.2:c.73T>A (PPP2R5D)	NP_001257405.1:p.Ser25Thr
NM_180976.3:c.430T>A (PPP2R5D)	NP_851307.1:p.Ser144Thr
NM_180977.3:c.208T>A (PPP2R5D)	NP_851308.1:p.Ser70Thr