Canonical Allele Identifier: CA891838029
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965425_87965427delinsGAA , CM000672.2:g.87965425_87965427delinsGAA GRCh38
NC_000010.10:g.89725182_89725184delinsGAA , CM000672.1:g.89725182_89725184delinsGAA GRCh37
NC_000010.9:g.89715162_89715164delinsGAA NCBI36
NG_007466.2:g.106987_106989delinsGAA , LRG_311:g.106987_106989delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1258_1260delinsGAA ENSP00000514759.2:p.Asn420Glu
ENST00000710265.1:c.*194_*196delinsGAA ENSP00000518161.1:n.*194_*196delinsGAA
ENST00000688158.2:n.1900_1902delinsGAA
ENST00000688922.2:c.*995_*997delinsGAA ENSP00000508742.2:n.*995_*997delinsGAA
ENST00000700021.1:c.1120_1122delinsGAA ENSP00000514757.1:p.Asn374Glu
ENST00000700022.1:c.*504_*506delinsGAA ENSP00000514758.1:n.*504_*506delinsGAA
ENST00000700023.1:n.2323_2325delinsGAA
ENST00000700024.1:n.2557_2559delinsGAA
ENST00000706954.1:c.1165_1167delinsGAA ENSP00000516674.1:p.Asn389Glu
ENST00000706955.1:c.*1200_*1202delinsGAA ENSP00000516675.1:n.*1200_*1202delinsGAA
ENST00000686459.1:c.*751_*753delinsGAA ENSP00000508909.1:n.*751_*753delinsGAA
ENST00000688158.1:c.*1276_*1278delinsGAA ENSP00000509254.1:n.*1276_*1278delinsGAA
ENST00000688308.1:c.1165_1167delinsGAA ENSP00000508752.1:p.Asn389Glu
ENST00000688922.1:c.1086_1088delinsGAA
ENST00000693560.1:c.1684_1686delinsGAA ENSP00000509861.1:p.Asn562Glu
ENST00000371953.8:c.1165_1167delinsGAA MANE Select ENSP00000361021.3:p.Asn389Glu
ENST00000371953.7:c.1165_1167delinsGAA ENSP00000361021.3:p.Asn389Glu
NM_000314.5:c.1165_1167delinsGAA NP_000305.3:p.Asn389Glu
NM_000314.6:c.1165_1167delinsGAA NP_000305.3:p.Asn389Glu
NM_001304717.2:c.1684_1686delinsGAA NP_001291646.2:p.Asn562Glu
NM_001304718.1:c.574_576delinsGAA NP_001291647.1:p.Asn192Glu
XM_006717926.2:c.1120_1122delinsGAA XP_006717989.1:p.Asn374Glu
XM_011539982.1:c.1069_1071delinsGAA XP_011538284.1:p.Asn357Glu
XR_945791.1:n.1735_1737delinsGAA
NM_000314.7:c.1165_1167delinsGAA NP_000305.3:p.Asn389Glu
NM_001304717.5:c.1684_1686delinsGAA NP_001291646.4:p.Asn562Glu
NM_001304718.2:c.574_576delinsGAA NP_001291647.1:p.Asn192Glu
NM_000314.8:c.1165_1167delinsGAA MANE Select NP_000305.3:p.Asn389Glu