Canonical Allele Identifier: CA891837563
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965368_87965369delinsCA , CM000672.2:g.87965368_87965369delinsCA GRCh38
NC_000010.10:g.89725125_89725126delinsCA , CM000672.1:g.89725125_89725126delinsCA GRCh37
NC_000010.9:g.89715105_89715106delinsCA NCBI36
NG_007466.2:g.106930_106931delinsCA , LRG_311:g.106930_106931delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1201_1202delinsCA ENSP00000514759.2:p.Ser401His
ENST00000710265.1:c.*137_*138delinsCA ENSP00000518161.1:n.*137_*138delinsCA
ENST00000688158.2:n.1843_1844delinsCA
ENST00000688922.2:c.*938_*939delinsCA ENSP00000508742.2:n.*938_*939delinsCA
ENST00000700021.1:c.1063_1064delinsCA ENSP00000514757.1:p.Ser355His
ENST00000700022.1:c.*447_*448delinsCA ENSP00000514758.1:n.*447_*448delinsCA
ENST00000700023.1:n.2266_2267delinsCA
ENST00000700024.1:n.2500_2501delinsCA
ENST00000706954.1:c.1108_1109delinsCA ENSP00000516674.1:p.Ser370His
ENST00000706955.1:c.*1143_*1144delinsCA ENSP00000516675.1:n.*1143_*1144delinsCA
ENST00000686459.1:c.*694_*695delinsCA ENSP00000508909.1:n.*694_*695delinsCA
ENST00000688158.1:c.*1219_*1220delinsCA ENSP00000509254.1:n.*1219_*1220delinsCA
ENST00000688308.1:c.1108_1109delinsCA ENSP00000508752.1:p.Ser370His
ENST00000688922.1:c.1029_1030delinsCA
ENST00000693560.1:c.1627_1628delinsCA ENSP00000509861.1:p.Ser543His
ENST00000371953.8:c.1108_1109delinsCA MANE Select ENSP00000361021.3:p.Ser370His
ENST00000371953.7:c.1108_1109delinsCA ENSP00000361021.3:p.Ser370His
NM_000314.5:c.1108_1109delinsCA NP_000305.3:p.Ser370His
NM_000314.6:c.1108_1109delinsCA NP_000305.3:p.Ser370His
NM_001304717.2:c.1627_1628delinsCA NP_001291646.2:p.Ser543His
NM_001304718.1:c.517_518delinsCA NP_001291647.1:p.Ser173His
XM_006717926.2:c.1063_1064delinsCA XP_006717989.1:p.Ser355His
XM_011539982.1:c.1012_1013delinsCA XP_011538284.1:p.Ser338His
XR_945791.1:n.1678_1679delinsCA
NM_000314.7:c.1108_1109delinsCA NP_000305.3:p.Ser370His
NM_001304717.5:c.1627_1628delinsCA NP_001291646.4:p.Ser543His
NM_001304718.2:c.517_518delinsCA NP_001291647.1:p.Ser173His
NM_000314.8:c.1108_1109delinsCA MANE Select NP_000305.3:p.Ser370His