Canonical Allele Identifier: CA470973807

Gene: PTEN

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961118G>A , CM000672.2:g.87961118G>A	GRCh38
NC_000010.10:g.89720875G>A , CM000672.1:g.89720875G>A	GRCh37
NC_000010.9:g.89710855G>A	NCBI36
NG_007466.2:g.102680G>A , LRG_311:g.102680G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1119G>A	ENSP00000514759.2:p.Lys373=
ENST00000710265.1:c.1026G>A	ENSP00000518161.1:p.Lys342=
ENST00000472832.3:c.1026G>A	ENSP00000483066.2:p.Lys342=
ENST00000688158.2:n.1761G>A
ENST00000688922.2:c.*856G>A	ENSP00000508742.2:n.*856G>A
ENST00000700021.1:c.981G>A	ENSP00000514757.1:p.Lys327=
ENST00000700022.1:c.*365G>A	ENSP00000514758.1:n.*365G>A
ENST00000700023.1:n.2184G>A
ENST00000700024.1:n.2418G>A
ENST00000700025.1:n.1795G>A
ENST00000700026.1:n.663G>A
ENST00000706954.1:c.1026G>A	ENSP00000516674.1:p.Lys342=
ENST00000706955.1:c.*1061G>A	ENSP00000516675.1:n.*1061G>A
ENST00000686459.1:c.*612G>A	ENSP00000508909.1:n.*612G>A
ENST00000688158.1:c.*1137G>A	ENSP00000509254.1:n.*1137G>A
ENST00000688308.1:c.1026G>A	ENSP00000508752.1:p.Lys342=
ENST00000688922.1:c.947G>A
ENST00000693560.1:c.1545G>A	ENSP00000509861.1:p.Lys515=
ENST00000371953.8:c.1026G>A MANE Select	ENSP00000361021.3:p.Lys342=
ENST00000371953.7:c.1026G>A	ENSP00000361021.3:p.Lys342=
ENST00000472832.2:c.453G>A	ENSP00000483066.1:p.Lys151=
NM_000314.5:c.1026G>A	NP_000305.3:p.Lys342=
NM_000314.6:c.1026G>A	NP_000305.3:p.Lys342=
NM_001304717.2:c.1545G>A	NP_001291646.2:p.Lys515=
NM_001304718.1:c.435G>A	NP_001291647.1:p.Lys145=
XM_006717926.2:c.981G>A	XP_006717989.1:p.Lys327=
XM_011539981.1:c.1026G>A	XP_011538283.1:p.Lys342=
XM_011539982.1:c.930G>A	XP_011538284.1:p.Lys310=
XR_945791.1:n.1596G>A
NM_000314.7:c.1026G>A	NP_000305.3:p.Lys342=
NM_001304717.5:c.1545G>A	NP_001291646.4:p.Lys515=
NM_001304718.2:c.435G>A	NP_001291647.1:p.Lys145=
NM_000314.8:c.1026G>A MANE Select	NP_000305.3:p.Lys342=