Canonical Allele Identifier: CA891839975
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957985_87957986delinsGT , CM000672.2:g.87957985_87957986delinsGT GRCh38
NC_000010.10:g.89717742_89717743delinsGT , CM000672.1:g.89717742_89717743delinsGT GRCh37
NC_000010.9:g.89707722_89707723delinsGT NCBI36
NG_007466.2:g.99547_99548delinsGT , LRG_311:g.99547_99548delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.767_768delinsGT ENSP00000514759.2:p.Glu256Gly
ENST00000710265.1:c.767_768delinsGT ENSP00000518161.1:p.Glu256Gly
ENST00000472832.3:c.767_768delinsGT ENSP00000483066.2:p.Glu256Gly
ENST00000688158.2:n.1502_1503delinsGT
ENST00000688922.2:c.*597_*598delinsGT ENSP00000508742.2:n.*597_*598delinsGT
ENST00000700021.1:c.722_723delinsGT ENSP00000514757.1:p.Glu241Gly
ENST00000700022.1:c.*106_*107delinsGT ENSP00000514758.1:n.*106_*107delinsGT
ENST00000700023.1:n.1925_1926delinsGT
ENST00000700024.1:n.2159_2160delinsGT
ENST00000700025.1:n.1536_1537delinsGT
ENST00000700026.1:n.404_405delinsGT
ENST00000700029.1:c.601_602delinsGT
ENST00000706954.1:c.767_768delinsGT ENSP00000516674.1:p.Glu256Gly
ENST00000706955.1:c.*802_*803delinsGT ENSP00000516675.1:n.*802_*803delinsGT
ENST00000686459.1:c.*353_*354delinsGT ENSP00000508909.1:n.*353_*354delinsGT
ENST00000688158.1:c.*878_*879delinsGT ENSP00000509254.1:n.*878_*879delinsGT
ENST00000688308.1:c.767_768delinsGT ENSP00000508752.1:p.Glu256Gly
ENST00000688922.1:c.688_689delinsGT
ENST00000693560.1:c.1286_1287delinsGT ENSP00000509861.1:p.Glu429Gly
ENST00000371953.8:c.767_768delinsGT MANE Select ENSP00000361021.3:p.Glu256Gly
ENST00000371953.7:c.767_768delinsGT ENSP00000361021.3:p.Glu256Gly
ENST00000472832.2:c.194_195delinsGT ENSP00000483066.1:p.Glu65Gly
NM_000314.5:c.767_768delinsGT NP_000305.3:p.Glu256Gly
NM_000314.6:c.767_768delinsGT NP_000305.3:p.Glu256Gly
NM_001304717.2:c.1286_1287delinsGT NP_001291646.2:p.Glu429Gly
NM_001304718.1:c.176_177delinsGT NP_001291647.1:p.Glu59Gly
XM_006717926.2:c.722_723delinsGT XP_006717989.1:p.Glu241Gly
XM_011539981.1:c.767_768delinsGT XP_011538283.1:p.Glu256Gly
XM_011539982.1:c.671_672delinsGT XP_011538284.1:p.Glu224Gly
XR_945791.1:n.1337_1338delinsGT
NM_000314.7:c.767_768delinsGT NP_000305.3:p.Glu256Gly
NM_001304717.5:c.1286_1287delinsGT NP_001291646.4:p.Glu429Gly
NM_001304718.2:c.176_177delinsGT NP_001291647.1:p.Glu59Gly
NM_000314.8:c.767_768delinsGT MANE Select NP_000305.3:p.Glu256Gly