Canonical Allele Identifier: CA891840023
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957996_87957998delinsGAT , CM000672.2:g.87957996_87957998delinsGAT GRCh38
NC_000010.10:g.89717753_89717755delinsGAT , CM000672.1:g.89717753_89717755delinsGAT GRCh37
NC_000010.9:g.89707733_89707735delinsGAT NCBI36
NG_007466.2:g.99558_99560delinsGAT , LRG_311:g.99558_99560delinsGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.778_780delinsGAT ENSP00000514759.2:p.Lys260Asp
ENST00000710265.1:c.778_780delinsGAT ENSP00000518161.1:p.Lys260Asp
ENST00000472832.3:c.778_780delinsGAT ENSP00000483066.2:p.Lys260Asp
ENST00000688158.2:n.1513_1515delinsGAT
ENST00000688922.2:c.*608_*610delinsGAT ENSP00000508742.2:n.*608_*610delinsGAT
ENST00000700021.1:c.733_735delinsGAT ENSP00000514757.1:p.Lys245Asp
ENST00000700022.1:c.*117_*119delinsGAT ENSP00000514758.1:n.*117_*119delinsGAT
ENST00000700023.1:n.1936_1938delinsGAT
ENST00000700024.1:n.2170_2172delinsGAT
ENST00000700025.1:n.1547_1549delinsGAT
ENST00000700026.1:n.415_417delinsGAT
ENST00000700029.1:c.612_614delinsGAT
ENST00000706954.1:c.778_780delinsGAT ENSP00000516674.1:p.Lys260Asp
ENST00000706955.1:c.*813_*815delinsGAT ENSP00000516675.1:n.*813_*815delinsGAT
ENST00000686459.1:c.*364_*366delinsGAT ENSP00000508909.1:n.*364_*366delinsGAT
ENST00000688158.1:c.*889_*891delinsGAT ENSP00000509254.1:n.*889_*891delinsGAT
ENST00000688308.1:c.778_780delinsGAT ENSP00000508752.1:p.Lys260Asp
ENST00000688922.1:c.699_701delinsGAT
ENST00000693560.1:c.1297_1299delinsGAT ENSP00000509861.1:p.Lys433Asp
ENST00000371953.8:c.778_780delinsGAT MANE Select ENSP00000361021.3:p.Lys260Asp
ENST00000371953.7:c.778_780delinsGAT ENSP00000361021.3:p.Lys260Asp
ENST00000472832.2:c.205_207delinsGAT ENSP00000483066.1:p.Lys69Asp
NM_000314.5:c.778_780delinsGAT NP_000305.3:p.Lys260Asp
NM_000314.6:c.778_780delinsGAT NP_000305.3:p.Lys260Asp
NM_001304717.2:c.1297_1299delinsGAT NP_001291646.2:p.Lys433Asp
NM_001304718.1:c.187_189delinsGAT NP_001291647.1:p.Lys63Asp
XM_006717926.2:c.733_735delinsGAT XP_006717989.1:p.Lys245Asp
XM_011539981.1:c.778_780delinsGAT XP_011538283.1:p.Lys260Asp
XM_011539982.1:c.682_684delinsGAT XP_011538284.1:p.Lys228Asp
XR_945791.1:n.1348_1350delinsGAT
NM_000314.7:c.778_780delinsGAT NP_000305.3:p.Lys260Asp
NM_001304717.5:c.1297_1299delinsGAT NP_001291646.4:p.Lys433Asp
NM_001304718.2:c.187_189delinsGAT NP_001291647.1:p.Lys63Asp
NM_000314.8:c.778_780delinsGAT MANE Select NP_000305.3:p.Lys260Asp