Canonical Allele Identifier: CA891837675
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965380_87965382delinsAAA , CM000672.2:g.87965380_87965382delinsAAA GRCh38
NC_000010.10:g.89725137_89725139delinsAAA , CM000672.1:g.89725137_89725139delinsAAA GRCh37
NC_000010.9:g.89715117_89715119delinsAAA NCBI36
NG_007466.2:g.106942_106944delinsAAA , LRG_311:g.106942_106944delinsAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1213_1215delinsAAA ENSP00000514759.2:p.Pro405Lys
ENST00000710265.1:c.*149_*151delinsAAA ENSP00000518161.1:n.*149_*151delinsAAA
ENST00000688158.2:n.1855_1857delinsAAA
ENST00000688922.2:c.*950_*952delinsAAA ENSP00000508742.2:n.*950_*952delinsAAA
ENST00000700021.1:c.1075_1077delinsAAA ENSP00000514757.1:p.Pro359Lys
ENST00000700022.1:c.*459_*461delinsAAA ENSP00000514758.1:n.*459_*461delinsAAA
ENST00000700023.1:n.2278_2280delinsAAA
ENST00000700024.1:n.2512_2514delinsAAA
ENST00000706954.1:c.1120_1122delinsAAA ENSP00000516674.1:p.Pro374Lys
ENST00000706955.1:c.*1155_*1157delinsAAA ENSP00000516675.1:n.*1155_*1157delinsAAA
ENST00000686459.1:c.*706_*708delinsAAA ENSP00000508909.1:n.*706_*708delinsAAA
ENST00000688158.1:c.*1231_*1233delinsAAA ENSP00000509254.1:n.*1231_*1233delinsAAA
ENST00000688308.1:c.1120_1122delinsAAA ENSP00000508752.1:p.Pro374Lys
ENST00000688922.1:c.1041_1043delinsAAA
ENST00000693560.1:c.1639_1641delinsAAA ENSP00000509861.1:p.Pro547Lys
ENST00000371953.8:c.1120_1122delinsAAA MANE Select ENSP00000361021.3:p.Pro374Lys
ENST00000371953.7:c.1120_1122delinsAAA ENSP00000361021.3:p.Pro374Lys
NM_000314.5:c.1120_1122delinsAAA NP_000305.3:p.Pro374Lys
NM_000314.6:c.1120_1122delinsAAA NP_000305.3:p.Pro374Lys
NM_001304717.2:c.1639_1641delinsAAA NP_001291646.2:p.Pro547Lys
NM_001304718.1:c.529_531delinsAAA NP_001291647.1:p.Pro177Lys
XM_006717926.2:c.1075_1077delinsAAA XP_006717989.1:p.Pro359Lys
XM_011539982.1:c.1024_1026delinsAAA XP_011538284.1:p.Pro342Lys
XR_945791.1:n.1690_1692delinsAAA
NM_000314.7:c.1120_1122delinsAAA NP_000305.3:p.Pro374Lys
NM_001304717.5:c.1639_1641delinsAAA NP_001291646.4:p.Pro547Lys
NM_001304718.2:c.529_531delinsAAA NP_001291647.1:p.Pro177Lys
NM_000314.8:c.1120_1122delinsAAA MANE Select NP_000305.3:p.Pro374Lys