Canonical Allele Identifier: CA891837566
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965368_87965369delinsGA , CM000672.2:g.87965368_87965369delinsGA GRCh38
NC_000010.10:g.89725125_89725126delinsGA , CM000672.1:g.89725125_89725126delinsGA GRCh37
NC_000010.9:g.89715105_89715106delinsGA NCBI36
NG_007466.2:g.106930_106931delinsGA , LRG_311:g.106930_106931delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1201_1202delinsGA ENSP00000514759.2:p.Ser401Asp
ENST00000710265.1:c.*137_*138delinsGA ENSP00000518161.1:n.*137_*138delinsGA
ENST00000688158.2:n.1843_1844delinsGA
ENST00000688922.2:c.*938_*939delinsGA ENSP00000508742.2:n.*938_*939delinsGA
ENST00000700021.1:c.1063_1064delinsGA ENSP00000514757.1:p.Ser355Asp
ENST00000700022.1:c.*447_*448delinsGA ENSP00000514758.1:n.*447_*448delinsGA
ENST00000700023.1:n.2266_2267delinsGA
ENST00000700024.1:n.2500_2501delinsGA
ENST00000706954.1:c.1108_1109delinsGA ENSP00000516674.1:p.Ser370Asp
ENST00000706955.1:c.*1143_*1144delinsGA ENSP00000516675.1:n.*1143_*1144delinsGA
ENST00000686459.1:c.*694_*695delinsGA ENSP00000508909.1:n.*694_*695delinsGA
ENST00000688158.1:c.*1219_*1220delinsGA ENSP00000509254.1:n.*1219_*1220delinsGA
ENST00000688308.1:c.1108_1109delinsGA ENSP00000508752.1:p.Ser370Asp
ENST00000688922.1:c.1029_1030delinsGA
ENST00000693560.1:c.1627_1628delinsGA ENSP00000509861.1:p.Ser543Asp
ENST00000371953.8:c.1108_1109delinsGA MANE Select ENSP00000361021.3:p.Ser370Asp
ENST00000371953.7:c.1108_1109delinsGA ENSP00000361021.3:p.Ser370Asp
NM_000314.5:c.1108_1109delinsGA NP_000305.3:p.Ser370Asp
NM_000314.6:c.1108_1109delinsGA NP_000305.3:p.Ser370Asp
NM_001304717.2:c.1627_1628delinsGA NP_001291646.2:p.Ser543Asp
NM_001304718.1:c.517_518delinsGA NP_001291647.1:p.Ser173Asp
XM_006717926.2:c.1063_1064delinsGA XP_006717989.1:p.Ser355Asp
XM_011539982.1:c.1012_1013delinsGA XP_011538284.1:p.Ser338Asp
XR_945791.1:n.1678_1679delinsGA
NM_000314.7:c.1108_1109delinsGA NP_000305.3:p.Ser370Asp
NM_001304717.5:c.1627_1628delinsGA NP_001291646.4:p.Ser543Asp
NM_001304718.2:c.517_518delinsGA NP_001291647.1:p.Ser173Asp
NM_000314.8:c.1108_1109delinsGA MANE Select NP_000305.3:p.Ser370Asp