Canonical Allele Identifier: CA891839840
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957957_87957959delinsATG , CM000672.2:g.87957957_87957959delinsATG GRCh38
NC_000010.10:g.89717714_89717716delinsATG , CM000672.1:g.89717714_89717716delinsATG GRCh37
NC_000010.9:g.89707694_89707696delinsATG NCBI36
NG_007466.2:g.99519_99521delinsATG , LRG_311:g.99519_99521delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.739_741delinsATG ENSP00000514759.2:p.Leu247Met
ENST00000710265.1:c.739_741delinsATG ENSP00000518161.1:p.Leu247Met
ENST00000472832.3:c.739_741delinsATG ENSP00000483066.2:p.Leu247Met
ENST00000688158.2:n.1474_1476delinsATG
ENST00000688922.2:c.*569_*571delinsATG ENSP00000508742.2:n.*569_*571delinsATG
ENST00000700021.1:c.694_696delinsATG ENSP00000514757.1:p.Leu232Met
ENST00000700022.1:c.*78_*80delinsATG ENSP00000514758.1:n.*78_*80delinsATG
ENST00000700023.1:n.1897_1899delinsATG
ENST00000700024.1:n.2131_2133delinsATG
ENST00000700025.1:n.1508_1510delinsATG
ENST00000700026.1:n.376_378delinsATG
ENST00000700029.1:c.573_575delinsATG
ENST00000706954.1:c.739_741delinsATG ENSP00000516674.1:p.Leu247Met
ENST00000706955.1:c.*774_*776delinsATG ENSP00000516675.1:n.*774_*776delinsATG
ENST00000686459.1:c.*325_*327delinsATG ENSP00000508909.1:n.*325_*327delinsATG
ENST00000688158.1:c.*850_*852delinsATG ENSP00000509254.1:n.*850_*852delinsATG
ENST00000688308.1:c.739_741delinsATG ENSP00000508752.1:p.Leu247Met
ENST00000688922.1:c.660_662delinsATG
ENST00000693560.1:c.1258_1260delinsATG ENSP00000509861.1:p.Leu420Met
ENST00000371953.8:c.739_741delinsATG MANE Select ENSP00000361021.3:p.Leu247Met
ENST00000371953.7:c.739_741delinsATG ENSP00000361021.3:p.Leu247Met
ENST00000472832.2:c.166_168delinsATG ENSP00000483066.1:p.Leu56Met
NM_000314.5:c.739_741delinsATG NP_000305.3:p.Leu247Met
NM_000314.6:c.739_741delinsATG NP_000305.3:p.Leu247Met
NM_001304717.2:c.1258_1260delinsATG NP_001291646.2:p.Leu420Met
NM_001304718.1:c.148_150delinsATG NP_001291647.1:p.Leu50Met
XM_006717926.2:c.694_696delinsATG XP_006717989.1:p.Leu232Met
XM_011539981.1:c.739_741delinsATG XP_011538283.1:p.Leu247Met
XM_011539982.1:c.643_645delinsATG XP_011538284.1:p.Leu215Met
XR_945791.1:n.1309_1311delinsATG
NM_000314.7:c.739_741delinsATG NP_000305.3:p.Leu247Met
NM_001304717.5:c.1258_1260delinsATG NP_001291646.4:p.Leu420Met
NM_001304718.2:c.148_150delinsATG NP_001291647.1:p.Leu50Met
NM_000314.8:c.739_741delinsATG MANE Select NP_000305.3:p.Leu247Met