Canonical Allele Identifier: CA891839871
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957963_87957965delinsTCT , CM000672.2:g.87957963_87957965delinsTCT GRCh38
NC_000010.10:g.89717720_89717722delinsTCT , CM000672.1:g.89717720_89717722delinsTCT GRCh37
NC_000010.9:g.89707700_89707702delinsTCT NCBI36
NG_007466.2:g.99525_99527delinsTCT , LRG_311:g.99525_99527delinsTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.745_747delinsTCT ENSP00000514759.2:p.Val249Ser
ENST00000710265.1:c.745_747delinsTCT ENSP00000518161.1:p.Val249Ser
ENST00000472832.3:c.745_747delinsTCT ENSP00000483066.2:p.Val249Ser
ENST00000688158.2:n.1480_1482delinsTCT
ENST00000688922.2:c.*575_*577delinsTCT ENSP00000508742.2:n.*575_*577delinsTCT
ENST00000700021.1:c.700_702delinsTCT ENSP00000514757.1:p.Val234Ser
ENST00000700022.1:c.*84_*86delinsTCT ENSP00000514758.1:n.*84_*86delinsTCT
ENST00000700023.1:n.1903_1905delinsTCT
ENST00000700024.1:n.2137_2139delinsTCT
ENST00000700025.1:n.1514_1516delinsTCT
ENST00000700026.1:n.382_384delinsTCT
ENST00000700029.1:c.579_581delinsTCT
ENST00000706954.1:c.745_747delinsTCT ENSP00000516674.1:p.Val249Ser
ENST00000706955.1:c.*780_*782delinsTCT ENSP00000516675.1:n.*780_*782delinsTCT
ENST00000686459.1:c.*331_*333delinsTCT ENSP00000508909.1:n.*331_*333delinsTCT
ENST00000688158.1:c.*856_*858delinsTCT ENSP00000509254.1:n.*856_*858delinsTCT
ENST00000688308.1:c.745_747delinsTCT ENSP00000508752.1:p.Val249Ser
ENST00000688922.1:c.666_668delinsTCT
ENST00000693560.1:c.1264_1266delinsTCT ENSP00000509861.1:p.Val422Ser
ENST00000371953.8:c.745_747delinsTCT MANE Select ENSP00000361021.3:p.Val249Ser
ENST00000371953.7:c.745_747delinsTCT ENSP00000361021.3:p.Val249Ser
ENST00000472832.2:c.172_174delinsTCT ENSP00000483066.1:p.Val58Ser
NM_000314.5:c.745_747delinsTCT NP_000305.3:p.Val249Ser
NM_000314.6:c.745_747delinsTCT NP_000305.3:p.Val249Ser
NM_001304717.2:c.1264_1266delinsTCT NP_001291646.2:p.Val422Ser
NM_001304718.1:c.154_156delinsTCT NP_001291647.1:p.Val52Ser
XM_006717926.2:c.700_702delinsTCT XP_006717989.1:p.Val234Ser
XM_011539981.1:c.745_747delinsTCT XP_011538283.1:p.Val249Ser
XM_011539982.1:c.649_651delinsTCT XP_011538284.1:p.Val217Ser
XR_945791.1:n.1315_1317delinsTCT
NM_000314.7:c.745_747delinsTCT NP_000305.3:p.Val249Ser
NM_001304717.5:c.1264_1266delinsTCT NP_001291646.4:p.Val422Ser
NM_001304718.2:c.154_156delinsTCT NP_001291647.1:p.Val52Ser
NM_000314.8:c.745_747delinsTCT MANE Select NP_000305.3:p.Val249Ser