Canonical Allele Identifier: CA891837577
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965368_87965369delinsGT , CM000672.2:g.87965368_87965369delinsGT GRCh38
NC_000010.10:g.89725125_89725126delinsGT , CM000672.1:g.89725125_89725126delinsGT GRCh37
NC_000010.9:g.89715105_89715106delinsGT NCBI36
NG_007466.2:g.106930_106931delinsGT , LRG_311:g.106930_106931delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1201_1202delinsGT ENSP00000514759.2:p.Ser401Val
ENST00000710265.1:c.*137_*138delinsGT ENSP00000518161.1:n.*137_*138delinsGT
ENST00000688158.2:n.1843_1844delinsGT
ENST00000688922.2:c.*938_*939delinsGT ENSP00000508742.2:n.*938_*939delinsGT
ENST00000700021.1:c.1063_1064delinsGT ENSP00000514757.1:p.Ser355Val
ENST00000700022.1:c.*447_*448delinsGT ENSP00000514758.1:n.*447_*448delinsGT
ENST00000700023.1:n.2266_2267delinsGT
ENST00000700024.1:n.2500_2501delinsGT
ENST00000706954.1:c.1108_1109delinsGT ENSP00000516674.1:p.Ser370Val
ENST00000706955.1:c.*1143_*1144delinsGT ENSP00000516675.1:n.*1143_*1144delinsGT
ENST00000686459.1:c.*694_*695delinsGT ENSP00000508909.1:n.*694_*695delinsGT
ENST00000688158.1:c.*1219_*1220delinsGT ENSP00000509254.1:n.*1219_*1220delinsGT
ENST00000688308.1:c.1108_1109delinsGT ENSP00000508752.1:p.Ser370Val
ENST00000688922.1:c.1029_1030delinsGT
ENST00000693560.1:c.1627_1628delinsGT ENSP00000509861.1:p.Ser543Val
ENST00000371953.8:c.1108_1109delinsGT MANE Select ENSP00000361021.3:p.Ser370Val
ENST00000371953.7:c.1108_1109delinsGT ENSP00000361021.3:p.Ser370Val
NM_000314.5:c.1108_1109delinsGT NP_000305.3:p.Ser370Val
NM_000314.6:c.1108_1109delinsGT NP_000305.3:p.Ser370Val
NM_001304717.2:c.1627_1628delinsGT NP_001291646.2:p.Ser543Val
NM_001304718.1:c.517_518delinsGT NP_001291647.1:p.Ser173Val
XM_006717926.2:c.1063_1064delinsGT XP_006717989.1:p.Ser355Val
XM_011539982.1:c.1012_1013delinsGT XP_011538284.1:p.Ser338Val
XR_945791.1:n.1678_1679delinsGT
NM_000314.7:c.1108_1109delinsGT NP_000305.3:p.Ser370Val
NM_001304717.5:c.1627_1628delinsGT NP_001291646.4:p.Ser543Val
NM_001304718.2:c.517_518delinsGT NP_001291647.1:p.Ser173Val
NM_000314.8:c.1108_1109delinsGT MANE Select NP_000305.3:p.Ser370Val