Canonical Allele Identifier: CA891841521
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965296_87965297delinsGC , CM000672.2:g.87965296_87965297delinsGC GRCh38
NC_000010.10:g.89725053_89725054delinsGC , CM000672.1:g.89725053_89725054delinsGC GRCh37
NC_000010.9:g.89715033_89715034delinsGC NCBI36
NG_007466.2:g.106858_106859delinsGC , LRG_311:g.106858_106859delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1129_1130delinsGC ENSP00000514759.2:p.Tyr377Ala
ENST00000710265.1:c.*65_*66delinsGC ENSP00000518161.1:n.*65_*66delinsGC
ENST00000688158.2:n.1771_1772delinsGC
ENST00000688922.2:c.*866_*867delinsGC ENSP00000508742.2:n.*866_*867delinsGC
ENST00000700021.1:c.991_992delinsGC ENSP00000514757.1:p.Tyr331Ala
ENST00000700022.1:c.*375_*376delinsGC ENSP00000514758.1:n.*375_*376delinsGC
ENST00000700023.1:n.2194_2195delinsGC
ENST00000700024.1:n.2428_2429delinsGC
ENST00000706954.1:c.1036_1037delinsGC ENSP00000516674.1:p.Tyr346Ala
ENST00000706955.1:c.*1071_*1072delinsGC ENSP00000516675.1:n.*1071_*1072delinsGC
ENST00000686459.1:c.*622_*623delinsGC ENSP00000508909.1:n.*622_*623delinsGC
ENST00000688158.1:c.*1147_*1148delinsGC ENSP00000509254.1:n.*1147_*1148delinsGC
ENST00000688308.1:c.1036_1037delinsGC ENSP00000508752.1:p.Tyr346Ala
ENST00000688922.1:c.957_958delinsGC
ENST00000693560.1:c.1555_1556delinsGC ENSP00000509861.1:p.Tyr519Ala
ENST00000371953.8:c.1036_1037delinsGC MANE Select ENSP00000361021.3:p.Tyr346Ala
ENST00000371953.7:c.1036_1037delinsGC ENSP00000361021.3:p.Tyr346Ala
NM_000314.5:c.1036_1037delinsGC NP_000305.3:p.Tyr346Ala
NM_000314.6:c.1036_1037delinsGC NP_000305.3:p.Tyr346Ala
NM_001304717.2:c.1555_1556delinsGC NP_001291646.2:p.Tyr519Ala
NM_001304718.1:c.445_446delinsGC NP_001291647.1:p.Tyr149Ala
XM_006717926.2:c.991_992delinsGC XP_006717989.1:p.Tyr331Ala
XM_011539982.1:c.940_941delinsGC XP_011538284.1:p.Tyr314Ala
XR_945791.1:n.1606_1607delinsGC
NM_000314.7:c.1036_1037delinsGC NP_000305.3:p.Tyr346Ala
NM_001304717.5:c.1555_1556delinsGC NP_001291646.4:p.Tyr519Ala
NM_001304718.2:c.445_446delinsGC NP_001291647.1:p.Tyr149Ala
NM_000314.8:c.1036_1037delinsGC MANE Select NP_000305.3:p.Tyr346Ala