Canonical Allele Identifier: CA891836345
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961030_87961031delinsTT , CM000672.2:g.87961030_87961031delinsTT GRCh38
NC_000010.10:g.89720787_89720788delinsTT , CM000672.1:g.89720787_89720788delinsTT GRCh37
NC_000010.9:g.89710767_89710768delinsTT NCBI36
NG_007466.2:g.102592_102593delinsTT , LRG_311:g.102592_102593delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1031_1032delinsTT ENSP00000514759.2:p.Lys344Ile
ENST00000710265.1:c.938_939delinsTT ENSP00000518161.1:p.Lys313Ile
ENST00000472832.3:c.938_939delinsTT ENSP00000483066.2:p.Lys313Ile
ENST00000688158.2:n.1673_1674delinsTT
ENST00000688922.2:c.*768_*769delinsTT ENSP00000508742.2:n.*768_*769delinsTT
ENST00000700021.1:c.893_894delinsTT ENSP00000514757.1:p.Lys298Ile
ENST00000700022.1:c.*277_*278delinsTT ENSP00000514758.1:n.*277_*278delinsTT
ENST00000700023.1:n.2096_2097delinsTT
ENST00000700024.1:n.2330_2331delinsTT
ENST00000700025.1:n.1707_1708delinsTT
ENST00000700026.1:n.575_576delinsTT
ENST00000706954.1:c.938_939delinsTT ENSP00000516674.1:p.Lys313Ile
ENST00000706955.1:c.*973_*974delinsTT ENSP00000516675.1:n.*973_*974delinsTT
ENST00000686459.1:c.*524_*525delinsTT ENSP00000508909.1:n.*524_*525delinsTT
ENST00000688158.1:c.*1049_*1050delinsTT ENSP00000509254.1:n.*1049_*1050delinsTT
ENST00000688308.1:c.938_939delinsTT ENSP00000508752.1:p.Lys313Ile
ENST00000688922.1:c.859_860delinsTT
ENST00000693560.1:c.1457_1458delinsTT ENSP00000509861.1:p.Lys486Ile
ENST00000371953.8:c.938_939delinsTT MANE Select ENSP00000361021.3:p.Lys313Ile
ENST00000371953.7:c.938_939delinsTT ENSP00000361021.3:p.Lys313Ile
ENST00000472832.2:c.365_366delinsTT ENSP00000483066.1:p.Lys122Ile
NM_000314.5:c.938_939delinsTT NP_000305.3:p.Lys313Ile
NM_000314.6:c.938_939delinsTT NP_000305.3:p.Lys313Ile
NM_001304717.2:c.1457_1458delinsTT NP_001291646.2:p.Lys486Ile
NM_001304718.1:c.347_348delinsTT NP_001291647.1:p.Lys116Ile
XM_006717926.2:c.893_894delinsTT XP_006717989.1:p.Lys298Ile
XM_011539981.1:c.938_939delinsTT XP_011538283.1:p.Lys313Ile
XM_011539982.1:c.842_843delinsTT XP_011538284.1:p.Lys281Ile
XR_945791.1:n.1508_1509delinsTT
NM_000314.7:c.938_939delinsTT NP_000305.3:p.Lys313Ile
NM_001304717.5:c.1457_1458delinsTT NP_001291646.4:p.Lys486Ile
NM_001304718.2:c.347_348delinsTT NP_001291647.1:p.Lys116Ile
NM_000314.8:c.938_939delinsTT MANE Select NP_000305.3:p.Lys313Ile