Canonical Allele Identifier: CA891839939
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957978_87957979delinsCC , CM000672.2:g.87957978_87957979delinsCC GRCh38
NC_000010.10:g.89717735_89717736delinsCC , CM000672.1:g.89717735_89717736delinsCC GRCh37
NC_000010.9:g.89707715_89707716delinsCC NCBI36
NG_007466.2:g.99540_99541delinsCC , LRG_311:g.99540_99541delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.760_761delinsCC ENSP00000514759.2:p.Lys254Pro
ENST00000710265.1:c.760_761delinsCC ENSP00000518161.1:p.Lys254Pro
ENST00000472832.3:c.760_761delinsCC ENSP00000483066.2:p.Lys254Pro
ENST00000688158.2:n.1495_1496delinsCC
ENST00000688922.2:c.*590_*591delinsCC ENSP00000508742.2:n.*590_*591delinsCC
ENST00000700021.1:c.715_716delinsCC ENSP00000514757.1:p.Lys239Pro
ENST00000700022.1:c.*99_*100delinsCC ENSP00000514758.1:n.*99_*100delinsCC
ENST00000700023.1:n.1918_1919delinsCC
ENST00000700024.1:n.2152_2153delinsCC
ENST00000700025.1:n.1529_1530delinsCC
ENST00000700026.1:n.397_398delinsCC
ENST00000700029.1:c.594_595delinsCC
ENST00000706954.1:c.760_761delinsCC ENSP00000516674.1:p.Lys254Pro
ENST00000706955.1:c.*795_*796delinsCC ENSP00000516675.1:n.*795_*796delinsCC
ENST00000686459.1:c.*346_*347delinsCC ENSP00000508909.1:n.*346_*347delinsCC
ENST00000688158.1:c.*871_*872delinsCC ENSP00000509254.1:n.*871_*872delinsCC
ENST00000688308.1:c.760_761delinsCC ENSP00000508752.1:p.Lys254Pro
ENST00000688922.1:c.681_682delinsCC
ENST00000693560.1:c.1279_1280delinsCC ENSP00000509861.1:p.Lys427Pro
ENST00000371953.8:c.760_761delinsCC MANE Select ENSP00000361021.3:p.Lys254Pro
ENST00000371953.7:c.760_761delinsCC ENSP00000361021.3:p.Lys254Pro
ENST00000472832.2:c.187_188delinsCC ENSP00000483066.1:p.Lys63Pro
NM_000314.5:c.760_761delinsCC NP_000305.3:p.Lys254Pro
NM_000314.6:c.760_761delinsCC NP_000305.3:p.Lys254Pro
NM_001304717.2:c.1279_1280delinsCC NP_001291646.2:p.Lys427Pro
NM_001304718.1:c.169_170delinsCC NP_001291647.1:p.Lys57Pro
XM_006717926.2:c.715_716delinsCC XP_006717989.1:p.Lys239Pro
XM_011539981.1:c.760_761delinsCC XP_011538283.1:p.Lys254Pro
XM_011539982.1:c.664_665delinsCC XP_011538284.1:p.Lys222Pro
XR_945791.1:n.1330_1331delinsCC
NM_000314.7:c.760_761delinsCC NP_000305.3:p.Lys254Pro
NM_001304717.5:c.1279_1280delinsCC NP_001291646.4:p.Lys427Pro
NM_001304718.2:c.169_170delinsCC NP_001291647.1:p.Lys57Pro
NM_000314.8:c.760_761delinsCC MANE Select NP_000305.3:p.Lys254Pro