Canonical Allele Identifier: CA891839889
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957966_87957968delinsATG , CM000672.2:g.87957966_87957968delinsATG GRCh38
NC_000010.10:g.89717723_89717725delinsATG , CM000672.1:g.89717723_89717725delinsATG GRCh37
NC_000010.9:g.89707703_89707705delinsATG NCBI36
NG_007466.2:g.99528_99530delinsATG , LRG_311:g.99528_99530delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.748_750delinsATG ENSP00000514759.2:p.Cys250Met
ENST00000710265.1:c.748_750delinsATG ENSP00000518161.1:p.Cys250Met
ENST00000472832.3:c.748_750delinsATG ENSP00000483066.2:p.Cys250Met
ENST00000688158.2:n.1483_1485delinsATG
ENST00000688922.2:c.*578_*580delinsATG ENSP00000508742.2:n.*578_*580delinsATG
ENST00000700021.1:c.703_705delinsATG ENSP00000514757.1:p.Cys235Met
ENST00000700022.1:c.*87_*89delinsATG ENSP00000514758.1:n.*87_*89delinsATG
ENST00000700023.1:n.1906_1908delinsATG
ENST00000700024.1:n.2140_2142delinsATG
ENST00000700025.1:n.1517_1519delinsATG
ENST00000700026.1:n.385_387delinsATG
ENST00000700029.1:c.582_584delinsATG
ENST00000706954.1:c.748_750delinsATG ENSP00000516674.1:p.Cys250Met
ENST00000706955.1:c.*783_*785delinsATG ENSP00000516675.1:n.*783_*785delinsATG
ENST00000686459.1:c.*334_*336delinsATG ENSP00000508909.1:n.*334_*336delinsATG
ENST00000688158.1:c.*859_*861delinsATG ENSP00000509254.1:n.*859_*861delinsATG
ENST00000688308.1:c.748_750delinsATG ENSP00000508752.1:p.Cys250Met
ENST00000688922.1:c.669_671delinsATG
ENST00000693560.1:c.1267_1269delinsATG ENSP00000509861.1:p.Cys423Met
ENST00000371953.8:c.748_750delinsATG MANE Select ENSP00000361021.3:p.Cys250Met
ENST00000371953.7:c.748_750delinsATG ENSP00000361021.3:p.Cys250Met
ENST00000472832.2:c.175_177delinsATG ENSP00000483066.1:p.Cys59Met
NM_000314.5:c.748_750delinsATG NP_000305.3:p.Cys250Met
NM_000314.6:c.748_750delinsATG NP_000305.3:p.Cys250Met
NM_001304717.2:c.1267_1269delinsATG NP_001291646.2:p.Cys423Met
NM_001304718.1:c.157_159delinsATG NP_001291647.1:p.Cys53Met
XM_006717926.2:c.703_705delinsATG XP_006717989.1:p.Cys235Met
XM_011539981.1:c.748_750delinsATG XP_011538283.1:p.Cys250Met
XM_011539982.1:c.652_654delinsATG XP_011538284.1:p.Cys218Met
XR_945791.1:n.1318_1320delinsATG
NM_000314.7:c.748_750delinsATG NP_000305.3:p.Cys250Met
NM_001304717.5:c.1267_1269delinsATG NP_001291646.4:p.Cys423Met
NM_001304718.2:c.157_159delinsATG NP_001291647.1:p.Cys53Met
NM_000314.8:c.748_750delinsATG MANE Select NP_000305.3:p.Cys250Met