Canonical Allele Identifier: CA891841486
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965290_87965291delinsTC , CM000672.2:g.87965290_87965291delinsTC GRCh38
NC_000010.10:g.89725047_89725048delinsTC , CM000672.1:g.89725047_89725048delinsTC GRCh37
NC_000010.9:g.89715027_89715028delinsTC NCBI36
NG_007466.2:g.106852_106853delinsTC , LRG_311:g.106852_106853delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1123_1124delinsTC ENSP00000514759.2:p.Lys375Ser
ENST00000710265.1:c.*59_*60delinsTC ENSP00000518161.1:n.*59_*60delinsTC
ENST00000688158.2:n.1765_1766delinsTC
ENST00000688922.2:c.*860_*861delinsTC ENSP00000508742.2:n.*860_*861delinsTC
ENST00000700021.1:c.985_986delinsTC ENSP00000514757.1:p.Lys329Ser
ENST00000700022.1:c.*369_*370delinsTC ENSP00000514758.1:n.*369_*370delinsTC
ENST00000700023.1:n.2188_2189delinsTC
ENST00000700024.1:n.2422_2423delinsTC
ENST00000706954.1:c.1030_1031delinsTC ENSP00000516674.1:p.Lys344Ser
ENST00000706955.1:c.*1065_*1066delinsTC ENSP00000516675.1:n.*1065_*1066delinsTC
ENST00000686459.1:c.*616_*617delinsTC ENSP00000508909.1:n.*616_*617delinsTC
ENST00000688158.1:c.*1141_*1142delinsTC ENSP00000509254.1:n.*1141_*1142delinsTC
ENST00000688308.1:c.1030_1031delinsTC ENSP00000508752.1:p.Lys344Ser
ENST00000688922.1:c.951_952delinsTC
ENST00000693560.1:c.1549_1550delinsTC ENSP00000509861.1:p.Lys517Ser
ENST00000371953.8:c.1030_1031delinsTC MANE Select ENSP00000361021.3:p.Lys344Ser
ENST00000371953.7:c.1030_1031delinsTC ENSP00000361021.3:p.Lys344Ser
NM_000314.5:c.1030_1031delinsTC NP_000305.3:p.Lys344Ser
NM_000314.6:c.1030_1031delinsTC NP_000305.3:p.Lys344Ser
NM_001304717.2:c.1549_1550delinsTC NP_001291646.2:p.Lys517Ser
NM_001304718.1:c.439_440delinsTC NP_001291647.1:p.Lys147Ser
XM_006717926.2:c.985_986delinsTC XP_006717989.1:p.Lys329Ser
XM_011539982.1:c.934_935delinsTC XP_011538284.1:p.Lys312Ser
XR_945791.1:n.1600_1601delinsTC
NM_000314.7:c.1030_1031delinsTC NP_000305.3:p.Lys344Ser
NM_001304717.5:c.1549_1550delinsTC NP_001291646.4:p.Lys517Ser
NM_001304718.2:c.439_440delinsTC NP_001291647.1:p.Lys147Ser
NM_000314.8:c.1030_1031delinsTC MANE Select NP_000305.3:p.Lys344Ser