Canonical Allele Identifier: CA891841605
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965365_87965366delinsCC , CM000672.2:g.87965365_87965366delinsCC GRCh38
NC_000010.10:g.89725122_89725123delinsCC , CM000672.1:g.89725122_89725123delinsCC GRCh37
NC_000010.9:g.89715102_89715103delinsCC NCBI36
NG_007466.2:g.106927_106928delinsCC , LRG_311:g.106927_106928delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1198_1199delinsCC ENSP00000514759.2:p.Val400Pro
ENST00000710265.1:c.*134_*135delinsCC ENSP00000518161.1:n.*134_*135delinsCC
ENST00000688158.2:n.1840_1841delinsCC
ENST00000688922.2:c.*935_*936delinsCC ENSP00000508742.2:n.*935_*936delinsCC
ENST00000700021.1:c.1060_1061delinsCC ENSP00000514757.1:p.Val354Pro
ENST00000700022.1:c.*444_*445delinsCC ENSP00000514758.1:n.*444_*445delinsCC
ENST00000700023.1:n.2263_2264delinsCC
ENST00000700024.1:n.2497_2498delinsCC
ENST00000706954.1:c.1105_1106delinsCC ENSP00000516674.1:p.Val369Pro
ENST00000706955.1:c.*1140_*1141delinsCC ENSP00000516675.1:n.*1140_*1141delinsCC
ENST00000686459.1:c.*691_*692delinsCC ENSP00000508909.1:n.*691_*692delinsCC
ENST00000688158.1:c.*1216_*1217delinsCC ENSP00000509254.1:n.*1216_*1217delinsCC
ENST00000688308.1:c.1105_1106delinsCC ENSP00000508752.1:p.Val369Pro
ENST00000688922.1:c.1026_1027delinsCC
ENST00000693560.1:c.1624_1625delinsCC ENSP00000509861.1:p.Val542Pro
ENST00000371953.8:c.1105_1106delinsCC MANE Select ENSP00000361021.3:p.Val369Pro
ENST00000371953.7:c.1105_1106delinsCC ENSP00000361021.3:p.Val369Pro
NM_000314.5:c.1105_1106delinsCC NP_000305.3:p.Val369Pro
NM_000314.6:c.1105_1106delinsCC NP_000305.3:p.Val369Pro
NM_001304717.2:c.1624_1625delinsCC NP_001291646.2:p.Val542Pro
NM_001304718.1:c.514_515delinsCC NP_001291647.1:p.Val172Pro
XM_006717926.2:c.1060_1061delinsCC XP_006717989.1:p.Val354Pro
XM_011539982.1:c.1009_1010delinsCC XP_011538284.1:p.Val337Pro
XR_945791.1:n.1675_1676delinsCC
NM_000314.7:c.1105_1106delinsCC NP_000305.3:p.Val369Pro
NM_001304717.5:c.1624_1625delinsCC NP_001291646.4:p.Val542Pro
NM_001304718.2:c.514_515delinsCC NP_001291647.1:p.Val172Pro
NM_000314.8:c.1105_1106delinsCC MANE Select NP_000305.3:p.Val369Pro