Canonical Allele Identifier: CA891837569
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965368_87965369delinsTA , CM000672.2:g.87965368_87965369delinsTA GRCh38
NC_000010.10:g.89725125_89725126delinsTA , CM000672.1:g.89725125_89725126delinsTA GRCh37
NC_000010.9:g.89715105_89715106delinsTA NCBI36
NG_007466.2:g.106930_106931delinsTA , LRG_311:g.106930_106931delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1201_1202delinsTA ENSP00000514759.2:p.Ser401Tyr
ENST00000710265.1:c.*137_*138delinsTA ENSP00000518161.1:n.*137_*138delinsTA
ENST00000688158.2:n.1843_1844delinsTA
ENST00000688922.2:c.*938_*939delinsTA ENSP00000508742.2:n.*938_*939delinsTA
ENST00000700021.1:c.1063_1064delinsTA ENSP00000514757.1:p.Ser355Tyr
ENST00000700022.1:c.*447_*448delinsTA ENSP00000514758.1:n.*447_*448delinsTA
ENST00000700023.1:n.2266_2267delinsTA
ENST00000700024.1:n.2500_2501delinsTA
ENST00000706954.1:c.1108_1109delinsTA ENSP00000516674.1:p.Ser370Tyr
ENST00000706955.1:c.*1143_*1144delinsTA ENSP00000516675.1:n.*1143_*1144delinsTA
ENST00000686459.1:c.*694_*695delinsTA ENSP00000508909.1:n.*694_*695delinsTA
ENST00000688158.1:c.*1219_*1220delinsTA ENSP00000509254.1:n.*1219_*1220delinsTA
ENST00000688308.1:c.1108_1109delinsTA ENSP00000508752.1:p.Ser370Tyr
ENST00000688922.1:c.1029_1030delinsTA
ENST00000693560.1:c.1627_1628delinsTA ENSP00000509861.1:p.Ser543Tyr
ENST00000371953.8:c.1108_1109delinsTA MANE Select ENSP00000361021.3:p.Ser370Tyr
ENST00000371953.7:c.1108_1109delinsTA ENSP00000361021.3:p.Ser370Tyr
NM_000314.5:c.1108_1109delinsTA NP_000305.3:p.Ser370Tyr
NM_000314.6:c.1108_1109delinsTA NP_000305.3:p.Ser370Tyr
NM_001304717.2:c.1627_1628delinsTA NP_001291646.2:p.Ser543Tyr
NM_001304718.1:c.517_518delinsTA NP_001291647.1:p.Ser173Tyr
XM_006717926.2:c.1063_1064delinsTA XP_006717989.1:p.Ser355Tyr
XM_011539982.1:c.1012_1013delinsTA XP_011538284.1:p.Ser338Tyr
XR_945791.1:n.1678_1679delinsTA
NM_000314.7:c.1108_1109delinsTA NP_000305.3:p.Ser370Tyr
NM_001304717.5:c.1627_1628delinsTA NP_001291646.4:p.Ser543Tyr
NM_001304718.2:c.517_518delinsTA NP_001291647.1:p.Ser173Tyr
NM_000314.8:c.1108_1109delinsTA MANE Select NP_000305.3:p.Ser370Tyr