Canonical Allele Identifier: CA2579926363
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965467_87965469delinsCCA , CM000672.2:g.87965467_87965469delinsCCA GRCh38
NC_000010.10:g.89725224_89725226delinsCCA , CM000672.1:g.89725224_89725226delinsCCA GRCh37
NC_000010.9:g.89715204_89715206delinsCCA NCBI36
NG_007466.2:g.107029_107031delinsCCA , LRG_311:g.107029_107031delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1300_1302delinsCCA ENSP00000514759.2:p.Val434Pro
ENST00000710265.1:c.*236_*238delinsCCA ENSP00000518161.1:n.*236_*238delinsCCA
ENST00000688158.2:n.1942_1944delinsCCA
ENST00000688922.2:c.*1037_*1039delinsCCA ENSP00000508742.2:n.*1037_*1039delinsCCA
ENST00000700021.1:c.1162_1164delinsCCA ENSP00000514757.1:p.Val388Pro
ENST00000700022.1:c.*546_*548delinsCCA ENSP00000514758.1:n.*546_*548delinsCCA
ENST00000700023.1:n.2365_2367delinsCCA
ENST00000700024.1:n.2599_2601delinsCCA
ENST00000706954.1:c.1207_1209delinsCCA ENSP00000516674.1:p.Val403Pro
ENST00000706955.1:c.*1242_*1244delinsCCA ENSP00000516675.1:n.*1242_*1244delinsCCA
ENST00000686459.1:c.*793_*795delinsCCA ENSP00000508909.1:n.*793_*795delinsCCA
ENST00000688158.1:c.*1318_*1320delinsCCA ENSP00000509254.1:n.*1318_*1320delinsCCA
ENST00000688308.1:c.1207_1209delinsCCA ENSP00000508752.1:p.Val403Pro
ENST00000688922.1:c.1128_1130delinsCCA
ENST00000693560.1:c.1726_1728delinsCCA ENSP00000509861.1:p.Val576Pro
ENST00000371953.8:c.1207_1209delinsCCA MANE Select ENSP00000361021.3:p.Val403Pro
ENST00000371953.7:c.1207_1209delinsCCA ENSP00000361021.3:p.Val403Pro
NM_000314.5:c.1207_1209delinsCCA NP_000305.3:p.Val403Pro
NM_000314.6:c.1207_1209delinsCCA NP_000305.3:p.Val403Pro
NM_001304717.2:c.1726_1728delinsCCA NP_001291646.2:p.Val576Pro
NM_001304718.1:c.616_618delinsCCA NP_001291647.1:p.Val206Pro
XM_006717926.2:c.1162_1164delinsCCA XP_006717989.1:p.Val388Pro
XM_011539982.1:c.1111_1113delinsCCA XP_011538284.1:p.Val371Pro
XR_945791.1:n.1777_1779delinsCCA
NM_000314.7:c.1207_1209delinsCCA NP_000305.3:p.Val403Pro
NM_001304717.5:c.1726_1728delinsCCA NP_001291646.4:p.Val576Pro
NM_001304718.2:c.616_618delinsCCA NP_001291647.1:p.Val206Pro
NM_000314.8:c.1207_1209delinsCCA MANE Select NP_000305.3:p.Val403Pro