Canonical Allele Identifier: CA377487390

Gene: PTEN

Linked Data

• MyVariant Identifiers: chr10:g.89725180A>C (hg19) ; chr10:g.87965423A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965423A>C , CM000672.2:g.87965423A>C	GRCh38
NC_000010.10:g.89725180A>C , CM000672.1:g.89725180A>C	GRCh37
NC_000010.9:g.89715160A>C	NCBI36
NG_007466.2:g.106985A>C , LRG_311:g.106985A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1256A>C	ENSP00000514759.2:p.Glu419Ala
ENST00000710265.1:c.*192A>C	ENSP00000518161.1:n.*192A>C
ENST00000688158.2:n.1898A>C
ENST00000688922.2:c.*993A>C	ENSP00000508742.2:n.*993A>C
ENST00000700021.1:c.1118A>C	ENSP00000514757.1:p.Glu373Ala
ENST00000700022.1:c.*502A>C	ENSP00000514758.1:n.*502A>C
ENST00000700023.1:n.2321A>C
ENST00000700024.1:n.2555A>C
ENST00000706954.1:c.1163A>C	ENSP00000516674.1:p.Glu388Ala
ENST00000706955.1:c.*1198A>C	ENSP00000516675.1:n.*1198A>C
ENST00000686459.1:c.*749A>C	ENSP00000508909.1:n.*749A>C
ENST00000688158.1:c.*1274A>C	ENSP00000509254.1:n.*1274A>C
ENST00000688308.1:c.1163A>C	ENSP00000508752.1:p.Glu388Ala
ENST00000688922.1:c.1084A>C
ENST00000693560.1:c.1682A>C	ENSP00000509861.1:p.Glu561Ala
ENST00000371953.8:c.1163A>C MANE Select	ENSP00000361021.3:p.Glu388Ala
ENST00000371953.7:c.1163A>C	ENSP00000361021.3:p.Glu388Ala
NM_000314.5:c.1163A>C	NP_000305.3:p.Glu388Ala
NM_000314.6:c.1163A>C	NP_000305.3:p.Glu388Ala
NM_001304717.2:c.1682A>C	NP_001291646.2:p.Glu561Ala
NM_001304718.1:c.572A>C	NP_001291647.1:p.Glu191Ala
XM_006717926.2:c.1118A>C	XP_006717989.1:p.Glu373Ala
XM_011539982.1:c.1067A>C	XP_011538284.1:p.Glu356Ala
XR_945791.1:n.1733A>C
NM_000314.7:c.1163A>C	NP_000305.3:p.Glu388Ala
NM_001304717.5:c.1682A>C	NP_001291646.4:p.Glu561Ala
NM_001304718.2:c.572A>C	NP_001291647.1:p.Glu191Ala
NM_000314.8:c.1163A>C MANE Select	NP_000305.3:p.Glu388Ala