Canonical Allele Identifier: CA891839814
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957954_87957956delinsTAA , CM000672.2:g.87957954_87957956delinsTAA GRCh38
NC_000010.10:g.89717711_89717713delinsTAA , CM000672.1:g.89717711_89717713delinsTAA GRCh37
NC_000010.9:g.89707691_89707693delinsTAA NCBI36
NG_007466.2:g.99516_99518delinsTAA , LRG_311:g.99516_99518delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.736_738delinsTAA ENSP00000514759.2:p.Pro246Ter
ENST00000710265.1:c.736_738delinsTAA ENSP00000518161.1:p.Pro246Ter
ENST00000472832.3:c.736_738delinsTAA ENSP00000483066.2:p.Pro246Ter
ENST00000688158.2:n.1471_1473delinsTAA
ENST00000688922.2:c.*566_*568delinsTAA ENSP00000508742.2:n.*566_*568delinsTAA
ENST00000700021.1:c.691_693delinsTAA ENSP00000514757.1:p.Pro231Ter
ENST00000700022.1:c.*75_*77delinsTAA ENSP00000514758.1:n.*75_*77delinsTAA
ENST00000700023.1:n.1894_1896delinsTAA
ENST00000700024.1:n.2128_2130delinsTAA
ENST00000700025.1:n.1505_1507delinsTAA
ENST00000700026.1:n.373_375delinsTAA
ENST00000700029.1:c.570_572delinsTAA
ENST00000706954.1:c.736_738delinsTAA ENSP00000516674.1:p.Pro246Ter
ENST00000706955.1:c.*771_*773delinsTAA ENSP00000516675.1:n.*771_*773delinsTAA
ENST00000686459.1:c.*322_*324delinsTAA ENSP00000508909.1:n.*322_*324delinsTAA
ENST00000688158.1:c.*847_*849delinsTAA ENSP00000509254.1:n.*847_*849delinsTAA
ENST00000688308.1:c.736_738delinsTAA ENSP00000508752.1:p.Pro246Ter
ENST00000688922.1:c.657_659delinsTAA
ENST00000693560.1:c.1255_1257delinsTAA ENSP00000509861.1:p.Pro419Ter
ENST00000371953.8:c.736_738delinsTAA MANE Select ENSP00000361021.3:p.Pro246Ter
ENST00000371953.7:c.736_738delinsTAA ENSP00000361021.3:p.Pro246Ter
ENST00000472832.2:c.163_165delinsTAA ENSP00000483066.1:p.Pro55Ter
NM_000314.5:c.736_738delinsTAA NP_000305.3:p.Pro246Ter
NM_000314.6:c.736_738delinsTAA NP_000305.3:p.Pro246Ter
NM_001304717.2:c.1255_1257delinsTAA NP_001291646.2:p.Pro419Ter
NM_001304718.1:c.145_147delinsTAA NP_001291647.1:p.Pro49Ter
XM_006717926.2:c.691_693delinsTAA XP_006717989.1:p.Pro231Ter
XM_011539981.1:c.736_738delinsTAA XP_011538283.1:p.Pro246Ter
XM_011539982.1:c.640_642delinsTAA XP_011538284.1:p.Pro214Ter
XR_945791.1:n.1306_1308delinsTAA
NM_000314.7:c.736_738delinsTAA NP_000305.3:p.Pro246Ter
NM_001304717.5:c.1255_1257delinsTAA NP_001291646.4:p.Pro419Ter
NM_001304718.2:c.145_147delinsTAA NP_001291647.1:p.Pro49Ter
NM_000314.8:c.736_738delinsTAA MANE Select NP_000305.3:p.Pro246Ter