Canonical Allele Identifier: CA891840809
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957954_87957955delinsAA , CM000672.2:g.87957954_87957955delinsAA GRCh38
NC_000010.10:g.89717711_89717712delinsAA , CM000672.1:g.89717711_89717712delinsAA GRCh37
NC_000010.9:g.89707691_89707692delinsAA NCBI36
NG_007466.2:g.99516_99517delinsAA , LRG_311:g.99516_99517delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.736_737delinsAA ENSP00000514759.2:p.Pro246Lys
ENST00000710265.1:c.736_737delinsAA ENSP00000518161.1:p.Pro246Lys
ENST00000472832.3:c.736_737delinsAA ENSP00000483066.2:p.Pro246Lys
ENST00000688158.2:n.1471_1472delinsAA
ENST00000688922.2:c.*566_*567delinsAA ENSP00000508742.2:n.*566_*567delinsAA
ENST00000700021.1:c.691_692delinsAA ENSP00000514757.1:p.Pro231Lys
ENST00000700022.1:c.*75_*76delinsAA ENSP00000514758.1:n.*75_*76delinsAA
ENST00000700023.1:n.1894_1895delinsAA
ENST00000700024.1:n.2128_2129delinsAA
ENST00000700025.1:n.1505_1506delinsAA
ENST00000700026.1:n.373_374delinsAA
ENST00000700029.1:c.570_571delinsAA
ENST00000706954.1:c.736_737delinsAA ENSP00000516674.1:p.Pro246Lys
ENST00000706955.1:c.*771_*772delinsAA ENSP00000516675.1:n.*771_*772delinsAA
ENST00000686459.1:c.*322_*323delinsAA ENSP00000508909.1:n.*322_*323delinsAA
ENST00000688158.1:c.*847_*848delinsAA ENSP00000509254.1:n.*847_*848delinsAA
ENST00000688308.1:c.736_737delinsAA ENSP00000508752.1:p.Pro246Lys
ENST00000688922.1:c.657_658delinsAA
ENST00000693560.1:c.1255_1256delinsAA ENSP00000509861.1:p.Pro419Lys
ENST00000371953.8:c.736_737delinsAA MANE Select ENSP00000361021.3:p.Pro246Lys
ENST00000371953.7:c.736_737delinsAA ENSP00000361021.3:p.Pro246Lys
ENST00000472832.2:c.163_164delinsAA ENSP00000483066.1:p.Pro55Lys
NM_000314.5:c.736_737delinsAA NP_000305.3:p.Pro246Lys
NM_000314.6:c.736_737delinsAA NP_000305.3:p.Pro246Lys
NM_001304717.2:c.1255_1256delinsAA NP_001291646.2:p.Pro419Lys
NM_001304718.1:c.145_146delinsAA NP_001291647.1:p.Pro49Lys
XM_006717926.2:c.691_692delinsAA XP_006717989.1:p.Pro231Lys
XM_011539981.1:c.736_737delinsAA XP_011538283.1:p.Pro246Lys
XM_011539982.1:c.640_641delinsAA XP_011538284.1:p.Pro214Lys
XR_945791.1:n.1306_1307delinsAA
NM_000314.7:c.736_737delinsAA NP_000305.3:p.Pro246Lys
NM_001304717.5:c.1255_1256delinsAA NP_001291646.4:p.Pro419Lys
NM_001304718.2:c.145_146delinsAA NP_001291647.1:p.Pro49Lys
NM_000314.8:c.736_737delinsAA MANE Select NP_000305.3:p.Pro246Lys