Canonical Allele Identifier: CA377485843
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132282700

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961009T>A , CM000672.2:g.87961009T>A GRCh38
NC_000010.10:g.89720766T>A , CM000672.1:g.89720766T>A GRCh37
NC_000010.9:g.89710746T>A NCBI36
NG_007466.2:g.102571T>A , LRG_311:g.102571T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1010T>A ENSP00000514759.2:p.Ile337Lys
ENST00000710265.1:c.917T>A ENSP00000518161.1:p.Ile306Lys
ENST00000472832.3:c.917T>A ENSP00000483066.2:p.Ile306Lys
ENST00000688158.2:n.1652T>A
ENST00000688922.2:c.*747T>A ENSP00000508742.2:n.*747T>A
ENST00000700021.1:c.872T>A ENSP00000514757.1:p.Ile291Lys
ENST00000700022.1:c.*256T>A ENSP00000514758.1:n.*256T>A
ENST00000700023.1:n.2075T>A
ENST00000700024.1:n.2309T>A
ENST00000700025.1:n.1686T>A
ENST00000700026.1:n.554T>A
ENST00000706954.1:c.917T>A ENSP00000516674.1:p.Ile306Lys
ENST00000706955.1:c.*952T>A ENSP00000516675.1:n.*952T>A
ENST00000686459.1:c.*503T>A ENSP00000508909.1:n.*503T>A
ENST00000688158.1:c.*1028T>A ENSP00000509254.1:n.*1028T>A
ENST00000688308.1:c.917T>A ENSP00000508752.1:p.Ile306Lys
ENST00000688922.1:c.838T>A
ENST00000693560.1:c.1436T>A ENSP00000509861.1:p.Ile479Lys
ENST00000371953.8:c.917T>A MANE Select ENSP00000361021.3:p.Ile306Lys
ENST00000371953.7:c.917T>A ENSP00000361021.3:p.Ile306Lys
ENST00000472832.2:c.344T>A ENSP00000483066.1:p.Ile115Lys
NM_000314.5:c.917T>A NP_000305.3:p.Ile306Lys
NM_000314.6:c.917T>A NP_000305.3:p.Ile306Lys
NM_001304717.2:c.1436T>A NP_001291646.2:p.Ile479Lys
NM_001304718.1:c.326T>A NP_001291647.1:p.Ile109Lys
XM_006717926.2:c.872T>A XP_006717989.1:p.Ile291Lys
XM_011539981.1:c.917T>A XP_011538283.1:p.Ile306Lys
XM_011539982.1:c.821T>A XP_011538284.1:p.Ile274Lys
XR_945791.1:n.1487T>A
NM_000314.7:c.917T>A NP_000305.3:p.Ile306Lys
NM_001304717.5:c.1436T>A NP_001291646.4:p.Ile479Lys
NM_001304718.2:c.326T>A NP_001291647.1:p.Ile109Lys
NM_000314.8:c.917T>A MANE Select NP_000305.3:p.Ile306Lys