Canonical Allele Identifier: CA891840812
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957954_87957955delinsGG , CM000672.2:g.87957954_87957955delinsGG GRCh38
NC_000010.10:g.89717711_89717712delinsGG , CM000672.1:g.89717711_89717712delinsGG GRCh37
NC_000010.9:g.89707691_89707692delinsGG NCBI36
NG_007466.2:g.99516_99517delinsGG , LRG_311:g.99516_99517delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.736_737delinsGG ENSP00000514759.2:p.Pro246Gly
ENST00000710265.1:c.736_737delinsGG ENSP00000518161.1:p.Pro246Gly
ENST00000472832.3:c.736_737delinsGG ENSP00000483066.2:p.Pro246Gly
ENST00000688158.2:n.1471_1472delinsGG
ENST00000688922.2:c.*566_*567delinsGG ENSP00000508742.2:n.*566_*567delinsGG
ENST00000700021.1:c.691_692delinsGG ENSP00000514757.1:p.Pro231Gly
ENST00000700022.1:c.*75_*76delinsGG ENSP00000514758.1:n.*75_*76delinsGG
ENST00000700023.1:n.1894_1895delinsGG
ENST00000700024.1:n.2128_2129delinsGG
ENST00000700025.1:n.1505_1506delinsGG
ENST00000700026.1:n.373_374delinsGG
ENST00000700029.1:c.570_571delinsGG
ENST00000706954.1:c.736_737delinsGG ENSP00000516674.1:p.Pro246Gly
ENST00000706955.1:c.*771_*772delinsGG ENSP00000516675.1:n.*771_*772delinsGG
ENST00000686459.1:c.*322_*323delinsGG ENSP00000508909.1:n.*322_*323delinsGG
ENST00000688158.1:c.*847_*848delinsGG ENSP00000509254.1:n.*847_*848delinsGG
ENST00000688308.1:c.736_737delinsGG ENSP00000508752.1:p.Pro246Gly
ENST00000688922.1:c.657_658delinsGG
ENST00000693560.1:c.1255_1256delinsGG ENSP00000509861.1:p.Pro419Gly
ENST00000371953.8:c.736_737delinsGG MANE Select ENSP00000361021.3:p.Pro246Gly
ENST00000371953.7:c.736_737delinsGG ENSP00000361021.3:p.Pro246Gly
ENST00000472832.2:c.163_164delinsGG ENSP00000483066.1:p.Pro55Gly
NM_000314.5:c.736_737delinsGG NP_000305.3:p.Pro246Gly
NM_000314.6:c.736_737delinsGG NP_000305.3:p.Pro246Gly
NM_001304717.2:c.1255_1256delinsGG NP_001291646.2:p.Pro419Gly
NM_001304718.1:c.145_146delinsGG NP_001291647.1:p.Pro49Gly
XM_006717926.2:c.691_692delinsGG XP_006717989.1:p.Pro231Gly
XM_011539981.1:c.736_737delinsGG XP_011538283.1:p.Pro246Gly
XM_011539982.1:c.640_641delinsGG XP_011538284.1:p.Pro214Gly
XR_945791.1:n.1306_1307delinsGG
NM_000314.7:c.736_737delinsGG NP_000305.3:p.Pro246Gly
NM_001304717.5:c.1255_1256delinsGG NP_001291646.4:p.Pro419Gly
NM_001304718.2:c.145_146delinsGG NP_001291647.1:p.Pro49Gly
NM_000314.8:c.736_737delinsGG MANE Select NP_000305.3:p.Pro246Gly