Canonical Allele Identifier: CA891841109
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960957_87960958delinsGG , CM000672.2:g.87960957_87960958delinsGG GRCh38
NC_000010.10:g.89720714_89720715delinsGG , CM000672.1:g.89720714_89720715delinsGG GRCh37
NC_000010.9:g.89710694_89710695delinsGG NCBI36
NG_007466.2:g.102519_102520delinsGG , LRG_311:g.102519_102520delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.958_959delinsGG ENSP00000514759.2:p.Lys320Gly
ENST00000710265.1:c.865_866delinsGG ENSP00000518161.1:p.Lys289Gly
ENST00000472832.3:c.865_866delinsGG ENSP00000483066.2:p.Lys289Gly
ENST00000688158.2:n.1600_1601delinsGG
ENST00000688922.2:c.*695_*696delinsGG ENSP00000508742.2:n.*695_*696delinsGG
ENST00000700021.1:c.820_821delinsGG ENSP00000514757.1:p.Lys274Gly
ENST00000700022.1:c.*204_*205delinsGG ENSP00000514758.1:n.*204_*205delinsGG
ENST00000700023.1:n.2023_2024delinsGG
ENST00000700024.1:n.2257_2258delinsGG
ENST00000700025.1:n.1634_1635delinsGG
ENST00000700026.1:n.502_503delinsGG
ENST00000700029.1:c.792_793delinsGG
ENST00000706954.1:c.865_866delinsGG ENSP00000516674.1:p.Lys289Gly
ENST00000706955.1:c.*900_*901delinsGG ENSP00000516675.1:n.*900_*901delinsGG
ENST00000686459.1:c.*451_*452delinsGG ENSP00000508909.1:n.*451_*452delinsGG
ENST00000688158.1:c.*976_*977delinsGG ENSP00000509254.1:n.*976_*977delinsGG
ENST00000688308.1:c.865_866delinsGG ENSP00000508752.1:p.Lys289Gly
ENST00000688922.1:c.786_787delinsGG
ENST00000693560.1:c.1384_1385delinsGG ENSP00000509861.1:p.Lys462Gly
ENST00000371953.8:c.865_866delinsGG MANE Select ENSP00000361021.3:p.Lys289Gly
ENST00000371953.7:c.865_866delinsGG ENSP00000361021.3:p.Lys289Gly
ENST00000472832.2:c.292_293delinsGG ENSP00000483066.1:p.Lys98Gly
NM_000314.5:c.865_866delinsGG NP_000305.3:p.Lys289Gly
NM_000314.6:c.865_866delinsGG NP_000305.3:p.Lys289Gly
NM_001304717.2:c.1384_1385delinsGG NP_001291646.2:p.Lys462Gly
NM_001304718.1:c.274_275delinsGG NP_001291647.1:p.Lys92Gly
XM_006717926.2:c.820_821delinsGG XP_006717989.1:p.Lys274Gly
XM_011539981.1:c.865_866delinsGG XP_011538283.1:p.Lys289Gly
XM_011539982.1:c.769_770delinsGG XP_011538284.1:p.Lys257Gly
XR_945791.1:n.1435_1436delinsGG
NM_000314.7:c.865_866delinsGG NP_000305.3:p.Lys289Gly
NM_001304717.5:c.1384_1385delinsGG NP_001291646.4:p.Lys462Gly
NM_001304718.2:c.274_275delinsGG NP_001291647.1:p.Lys92Gly
NM_000314.8:c.865_866delinsGG MANE Select NP_000305.3:p.Lys289Gly