Canonical Allele Identifier: CA000129

Gene: PTEN

Linked Data

• ClinVar Variation Id: 187590
• ClinVar RCV Id: RCV000167333 ; RCV000212879 ; RCV000710306 ; RCV002288765
• dbSNP Id: rs786203847
• COSMIC: COSM5960
• MyVariant Identifiers: chr10:g.89685269G>A (hg19) ; chr10:g.87925512G>A (hg38)
• ERepo: CA000129/MONDO:0017623/003
• PubMed: PMID:21194675

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925512G>A , CM000672.2:g.87925512G>A	GRCh38
NC_000010.10:g.89685269G>A , CM000672.1:g.89685269G>A	GRCh37
NC_000010.9:g.89675249G>A	NCBI36
NG_007466.2:g.67074G>A , LRG_311:g.67074G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.165-1G>A	ENSP00000514759.2:n.165-1G>A
ENST00000710265.1:c.165-1G>A	ENSP00000518161.1:n.165-1G>A
ENST00000472832.3:c.165-1G>A	ENSP00000483066.2:n.165-1G>A
ENST00000688158.2:n.900-1G>A
ENST00000688922.2:c.165-1G>A	ENSP00000508742.2:n.165-1G>A
ENST00000700021.1:c.165-5534G>A	ENSP00000514757.1:n.165-5534G>A
ENST00000700022.1:c.165-1G>A	ENSP00000514758.1:n.165-1G>A
ENST00000706954.1:c.165-1G>A	ENSP00000516674.1:n.165-1G>A
ENST00000706955.1:c.*200-1G>A	ENSP00000516675.1:n.*200-1G>A
ENST00000686459.1:c.165-1G>A	ENSP00000508909.1:n.165-1G>A
ENST00000688158.1:c.*276-1G>A	ENSP00000509254.1:n.*276-1G>A
ENST00000688308.1:c.165-1G>A	ENSP00000508752.1:n.165-1G>A
ENST00000688922.1:c.34-1G>A
ENST00000693560.1:c.684-1G>A	ENSP00000509861.1:n.684-1G>A
ENST00000371953.8:c.165-1G>A MANE Select	ENSP00000361021.3:n.165-1G>A
ENST00000371953.7:c.165-1G>A	ENSP00000361021.3:n.165-1G>A
ENST00000610634.1:c.63-1G>A	ENSP00000477517.1:n.63-1G>A
NM_000314.5:c.165-1G>A	NP_000305.3:n.165-1G>A
NM_000314.6:c.165-1G>A	NP_000305.3:n.165-1G>A
NM_001304717.2:c.684-1G>A	NP_001291646.2:n.684-1G>A
NM_001304718.1:c.-541-5534G>A	NP_001291647.1:n.-541-5534G>A
XM_006717926.2:c.165-5534G>A	XP_006717989.1:n.165-5534G>A
XM_011539981.1:c.165-1G>A	XP_011538283.1:n.165-1G>A
XM_011539982.1:c.69-1G>A	XP_011538284.1:n.69-1G>A
XR_945789.1:n.877-1G>A
XR_945790.1:n.877-1G>A
XR_945791.1:n.877-1G>A
NM_000314.7:c.165-1G>A	NP_000305.3:n.165-1G>A
NM_001304717.5:c.684-1G>A	NP_001291646.4:n.684-1G>A
NM_001304718.2:c.-541-5534G>A	NP_001291647.1:n.-541-5534G>A
NM_000314.8:c.165-1G>A MANE Select	NP_000305.3:n.165-1G>A