Canonical Allele Identifier: CA891841619
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965374_87965375delinsCC , CM000672.2:g.87965374_87965375delinsCC GRCh38
NC_000010.10:g.89725131_89725132delinsCC , CM000672.1:g.89725131_89725132delinsCC GRCh37
NC_000010.9:g.89715111_89715112delinsCC NCBI36
NG_007466.2:g.106936_106937delinsCC , LRG_311:g.106936_106937delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1207_1208delinsCC ENSP00000514759.2:p.Asn403Pro
ENST00000710265.1:c.*143_*144delinsCC ENSP00000518161.1:n.*143_*144delinsCC
ENST00000688158.2:n.1849_1850delinsCC
ENST00000688922.2:c.*944_*945delinsCC ENSP00000508742.2:n.*944_*945delinsCC
ENST00000700021.1:c.1069_1070delinsCC ENSP00000514757.1:p.Asn357Pro
ENST00000700022.1:c.*453_*454delinsCC ENSP00000514758.1:n.*453_*454delinsCC
ENST00000700023.1:n.2272_2273delinsCC
ENST00000700024.1:n.2506_2507delinsCC
ENST00000706954.1:c.1114_1115delinsCC ENSP00000516674.1:p.Asn372Pro
ENST00000706955.1:c.*1149_*1150delinsCC ENSP00000516675.1:n.*1149_*1150delinsCC
ENST00000686459.1:c.*700_*701delinsCC ENSP00000508909.1:n.*700_*701delinsCC
ENST00000688158.1:c.*1225_*1226delinsCC ENSP00000509254.1:n.*1225_*1226delinsCC
ENST00000688308.1:c.1114_1115delinsCC ENSP00000508752.1:p.Asn372Pro
ENST00000688922.1:c.1035_1036delinsCC
ENST00000693560.1:c.1633_1634delinsCC ENSP00000509861.1:p.Asn545Pro
ENST00000371953.8:c.1114_1115delinsCC MANE Select ENSP00000361021.3:p.Asn372Pro
ENST00000371953.7:c.1114_1115delinsCC ENSP00000361021.3:p.Asn372Pro
NM_000314.5:c.1114_1115delinsCC NP_000305.3:p.Asn372Pro
NM_000314.6:c.1114_1115delinsCC NP_000305.3:p.Asn372Pro
NM_001304717.2:c.1633_1634delinsCC NP_001291646.2:p.Asn545Pro
NM_001304718.1:c.523_524delinsCC NP_001291647.1:p.Asn175Pro
XM_006717926.2:c.1069_1070delinsCC XP_006717989.1:p.Asn357Pro
XM_011539982.1:c.1018_1019delinsCC XP_011538284.1:p.Asn340Pro
XR_945791.1:n.1684_1685delinsCC
NM_000314.7:c.1114_1115delinsCC NP_000305.3:p.Asn372Pro
NM_001304717.5:c.1633_1634delinsCC NP_001291646.4:p.Asn545Pro
NM_001304718.2:c.523_524delinsCC NP_001291647.1:p.Asn175Pro
NM_000314.8:c.1114_1115delinsCC MANE Select NP_000305.3:p.Asn372Pro