Canonical Allele Identifier: CA891834882
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960939_87960940delinsAA , CM000672.2:g.87960939_87960940delinsAA GRCh38
NC_000010.10:g.89720696_89720697delinsAA , CM000672.1:g.89720696_89720697delinsAA GRCh37
NC_000010.9:g.89710676_89710677delinsAA NCBI36
NG_007466.2:g.102501_102502delinsAA , LRG_311:g.102501_102502delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.940_941delinsAA ENSP00000514759.2:p.Pro314Lys
ENST00000710265.1:c.847_848delinsAA ENSP00000518161.1:p.Pro283Lys
ENST00000472832.3:c.847_848delinsAA ENSP00000483066.2:p.Pro283Lys
ENST00000688158.2:n.1582_1583delinsAA
ENST00000688922.2:c.*677_*678delinsAA ENSP00000508742.2:n.*677_*678delinsAA
ENST00000700021.1:c.802_803delinsAA ENSP00000514757.1:p.Pro268Lys
ENST00000700022.1:c.*186_*187delinsAA ENSP00000514758.1:n.*186_*187delinsAA
ENST00000700023.1:n.2005_2006delinsAA
ENST00000700024.1:n.2239_2240delinsAA
ENST00000700025.1:n.1616_1617delinsAA
ENST00000700026.1:n.484_485delinsAA
ENST00000700029.1:c.774_775delinsAA
ENST00000706954.1:c.847_848delinsAA ENSP00000516674.1:p.Pro283Lys
ENST00000706955.1:c.*882_*883delinsAA ENSP00000516675.1:n.*882_*883delinsAA
ENST00000686459.1:c.*433_*434delinsAA ENSP00000508909.1:n.*433_*434delinsAA
ENST00000688158.1:c.*958_*959delinsAA ENSP00000509254.1:n.*958_*959delinsAA
ENST00000688308.1:c.847_848delinsAA ENSP00000508752.1:p.Pro283Lys
ENST00000688922.1:c.768_769delinsAA
ENST00000693560.1:c.1366_1367delinsAA ENSP00000509861.1:p.Pro456Lys
ENST00000371953.8:c.847_848delinsAA MANE Select ENSP00000361021.3:p.Pro283Lys
ENST00000371953.7:c.847_848delinsAA ENSP00000361021.3:p.Pro283Lys
ENST00000472832.2:c.274_275delinsAA ENSP00000483066.1:p.Pro92Lys
NM_000314.5:c.847_848delinsAA NP_000305.3:p.Pro283Lys
NM_000314.6:c.847_848delinsAA NP_000305.3:p.Pro283Lys
NM_001304717.2:c.1366_1367delinsAA NP_001291646.2:p.Pro456Lys
NM_001304718.1:c.256_257delinsAA NP_001291647.1:p.Pro86Lys
XM_006717926.2:c.802_803delinsAA XP_006717989.1:p.Pro268Lys
XM_011539981.1:c.847_848delinsAA XP_011538283.1:p.Pro283Lys
XM_011539982.1:c.751_752delinsAA XP_011538284.1:p.Pro251Lys
XR_945791.1:n.1417_1418delinsAA
NM_000314.7:c.847_848delinsAA NP_000305.3:p.Pro283Lys
NM_001304717.5:c.1366_1367delinsAA NP_001291646.4:p.Pro456Lys
NM_001304718.2:c.256_257delinsAA NP_001291647.1:p.Pro86Lys
NM_000314.8:c.847_848delinsAA MANE Select NP_000305.3:p.Pro283Lys