Canonical Allele Identifier: CA891839875
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957963_87957965delinsATT , CM000672.2:g.87957963_87957965delinsATT GRCh38
NC_000010.10:g.89717720_89717722delinsATT , CM000672.1:g.89717720_89717722delinsATT GRCh37
NC_000010.9:g.89707700_89707702delinsATT NCBI36
NG_007466.2:g.99525_99527delinsATT , LRG_311:g.99525_99527delinsATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.745_747delinsATT ENSP00000514759.2:p.Val249Ile
ENST00000710265.1:c.745_747delinsATT ENSP00000518161.1:p.Val249Ile
ENST00000472832.3:c.745_747delinsATT ENSP00000483066.2:p.Val249Ile
ENST00000688158.2:n.1480_1482delinsATT
ENST00000688922.2:c.*575_*577delinsATT ENSP00000508742.2:n.*575_*577delinsATT
ENST00000700021.1:c.700_702delinsATT ENSP00000514757.1:p.Val234Ile
ENST00000700022.1:c.*84_*86delinsATT ENSP00000514758.1:n.*84_*86delinsATT
ENST00000700023.1:n.1903_1905delinsATT
ENST00000700024.1:n.2137_2139delinsATT
ENST00000700025.1:n.1514_1516delinsATT
ENST00000700026.1:n.382_384delinsATT
ENST00000700029.1:c.579_581delinsATT
ENST00000706954.1:c.745_747delinsATT ENSP00000516674.1:p.Val249Ile
ENST00000706955.1:c.*780_*782delinsATT ENSP00000516675.1:n.*780_*782delinsATT
ENST00000686459.1:c.*331_*333delinsATT ENSP00000508909.1:n.*331_*333delinsATT
ENST00000688158.1:c.*856_*858delinsATT ENSP00000509254.1:n.*856_*858delinsATT
ENST00000688308.1:c.745_747delinsATT ENSP00000508752.1:p.Val249Ile
ENST00000688922.1:c.666_668delinsATT
ENST00000693560.1:c.1264_1266delinsATT ENSP00000509861.1:p.Val422Ile
ENST00000371953.8:c.745_747delinsATT MANE Select ENSP00000361021.3:p.Val249Ile
ENST00000371953.7:c.745_747delinsATT ENSP00000361021.3:p.Val249Ile
ENST00000472832.2:c.172_174delinsATT ENSP00000483066.1:p.Val58Ile
NM_000314.5:c.745_747delinsATT NP_000305.3:p.Val249Ile
NM_000314.6:c.745_747delinsATT NP_000305.3:p.Val249Ile
NM_001304717.2:c.1264_1266delinsATT NP_001291646.2:p.Val422Ile
NM_001304718.1:c.154_156delinsATT NP_001291647.1:p.Val52Ile
XM_006717926.2:c.700_702delinsATT XP_006717989.1:p.Val234Ile
XM_011539981.1:c.745_747delinsATT XP_011538283.1:p.Val249Ile
XM_011539982.1:c.649_651delinsATT XP_011538284.1:p.Val217Ile
XR_945791.1:n.1315_1317delinsATT
NM_000314.7:c.745_747delinsATT NP_000305.3:p.Val249Ile
NM_001304717.5:c.1264_1266delinsATT NP_001291646.4:p.Val422Ile
NM_001304718.2:c.154_156delinsATT NP_001291647.1:p.Val52Ile
NM_000314.8:c.745_747delinsATT MANE Select NP_000305.3:p.Val249Ile