Canonical Allele Identifier: CA891839829
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957954_87957956delinsTAT , CM000672.2:g.87957954_87957956delinsTAT GRCh38
NC_000010.10:g.89717711_89717713delinsTAT , CM000672.1:g.89717711_89717713delinsTAT GRCh37
NC_000010.9:g.89707691_89707693delinsTAT NCBI36
NG_007466.2:g.99516_99518delinsTAT , LRG_311:g.99516_99518delinsTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.736_738delinsTAT ENSP00000514759.2:p.Pro246Tyr
ENST00000710265.1:c.736_738delinsTAT ENSP00000518161.1:p.Pro246Tyr
ENST00000472832.3:c.736_738delinsTAT ENSP00000483066.2:p.Pro246Tyr
ENST00000688158.2:n.1471_1473delinsTAT
ENST00000688922.2:c.*566_*568delinsTAT ENSP00000508742.2:n.*566_*568delinsTAT
ENST00000700021.1:c.691_693delinsTAT ENSP00000514757.1:p.Pro231Tyr
ENST00000700022.1:c.*75_*77delinsTAT ENSP00000514758.1:n.*75_*77delinsTAT
ENST00000700023.1:n.1894_1896delinsTAT
ENST00000700024.1:n.2128_2130delinsTAT
ENST00000700025.1:n.1505_1507delinsTAT
ENST00000700026.1:n.373_375delinsTAT
ENST00000700029.1:c.570_572delinsTAT
ENST00000706954.1:c.736_738delinsTAT ENSP00000516674.1:p.Pro246Tyr
ENST00000706955.1:c.*771_*773delinsTAT ENSP00000516675.1:n.*771_*773delinsTAT
ENST00000686459.1:c.*322_*324delinsTAT ENSP00000508909.1:n.*322_*324delinsTAT
ENST00000688158.1:c.*847_*849delinsTAT ENSP00000509254.1:n.*847_*849delinsTAT
ENST00000688308.1:c.736_738delinsTAT ENSP00000508752.1:p.Pro246Tyr
ENST00000688922.1:c.657_659delinsTAT
ENST00000693560.1:c.1255_1257delinsTAT ENSP00000509861.1:p.Pro419Tyr
ENST00000371953.8:c.736_738delinsTAT MANE Select ENSP00000361021.3:p.Pro246Tyr
ENST00000371953.7:c.736_738delinsTAT ENSP00000361021.3:p.Pro246Tyr
ENST00000472832.2:c.163_165delinsTAT ENSP00000483066.1:p.Pro55Tyr
NM_000314.5:c.736_738delinsTAT NP_000305.3:p.Pro246Tyr
NM_000314.6:c.736_738delinsTAT NP_000305.3:p.Pro246Tyr
NM_001304717.2:c.1255_1257delinsTAT NP_001291646.2:p.Pro419Tyr
NM_001304718.1:c.145_147delinsTAT NP_001291647.1:p.Pro49Tyr
XM_006717926.2:c.691_693delinsTAT XP_006717989.1:p.Pro231Tyr
XM_011539981.1:c.736_738delinsTAT XP_011538283.1:p.Pro246Tyr
XM_011539982.1:c.640_642delinsTAT XP_011538284.1:p.Pro214Tyr
XR_945791.1:n.1306_1308delinsTAT
NM_000314.7:c.736_738delinsTAT NP_000305.3:p.Pro246Tyr
NM_001304717.5:c.1255_1257delinsTAT NP_001291646.4:p.Pro419Tyr
NM_001304718.2:c.145_147delinsTAT NP_001291647.1:p.Pro49Tyr
NM_000314.8:c.736_738delinsTAT MANE Select NP_000305.3:p.Pro246Tyr