Canonical Allele Identifier: CA377781832

Gene: PTEN

Linked Data

• ClinVar Variation Id: 493079
• ClinVar RCV Id: RCV000585486 ; RCV003451323
• dbSNP Id: rs1554890335
• COSMIC: COSM5298
• MyVariant Identifiers: chr10:g.89624245G>T (hg19) ; chr10:g.87864488G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87864488G>T , CM000672.2:g.87864488G>T	GRCh38
NC_000010.10:g.89624245G>T , CM000672.1:g.89624245G>T	GRCh37
NC_000010.9:g.89614225G>T	NCBI36
NG_007466.2:g.6050G>T , LRG_311:g.6050G>T
NG_033079.1:g.3950C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.19G>T	ENSP00000514759.2:p.Glu7Ter
ENST00000710265.1:c.19G>T	ENSP00000518161.1:p.Glu7Ter
ENST00000472832.3:c.19G>T	ENSP00000483066.2:p.Glu7Ter
ENST00000688922.2:c.19G>T	ENSP00000508742.2:p.Glu7Ter
ENST00000700021.1:c.19G>T	ENSP00000514757.1:p.Glu7Ter
ENST00000700022.1:c.19G>T	ENSP00000514758.1:p.Glu7Ter
ENST00000706954.1:c.19G>T	ENSP00000516674.1:p.Glu7Ter
ENST00000706955.1:c.19G>T	ENSP00000516675.1:p.Glu7Ter
ENST00000686459.1:c.19G>T	ENSP00000508909.1:p.Glu7Ter
ENST00000688158.1:c.19G>T	ENSP00000509254.1:p.Glu7Ter
ENST00000688308.1:c.19G>T	ENSP00000508752.1:p.Glu7Ter
ENST00000693560.1:c.538G>T	ENSP00000509861.1:p.Glu180Ter
ENST00000371953.8:c.19G>T MANE Select	ENSP00000361021.3:p.Glu7Ter
ENST00000371953.7:c.19G>T	ENSP00000361021.3:p.Glu7Ter
ENST00000462694.1:n.21G>T
ENST00000487939.1:n.40G>T
ENST00000610634.1:c.-84G>T	ENSP00000477517.1:n.-84G>T
NM_000314.5:c.19G>T	NP_000305.3:p.Glu7Ter
NM_000314.6:c.19G>T	NP_000305.3:p.Glu7Ter
NM_001304717.2:c.538G>T	NP_001291646.2:p.Glu180Ter
NM_001304718.1:c.-687G>T	NP_001291647.1:n.-687G>T
XM_006717926.2:c.19G>T	XP_006717989.1:p.Glu7Ter
XM_011539981.1:c.19G>T	XP_011538283.1:p.Glu7Ter
XR_945789.1:n.731G>T
XR_945790.1:n.731G>T
XR_945791.1:n.731G>T
NM_000314.7:c.19G>T	NP_000305.3:p.Glu7Ter
NM_001304717.5:c.538G>T	NP_001291646.4:p.Glu180Ter
NM_001304718.2:c.-687G>T	NP_001291647.1:n.-687G>T
NM_000314.8:c.19G>T MANE Select	NP_000305.3:p.Glu7Ter