Canonical Allele Identifier: CA891838033
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965425_87965427delinsCAA , CM000672.2:g.87965425_87965427delinsCAA GRCh38
NC_000010.10:g.89725182_89725184delinsCAA , CM000672.1:g.89725182_89725184delinsCAA GRCh37
NC_000010.9:g.89715162_89715164delinsCAA NCBI36
NG_007466.2:g.106987_106989delinsCAA , LRG_311:g.106987_106989delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1258_1260delinsCAA ENSP00000514759.2:p.Asn420Gln
ENST00000710265.1:c.*194_*196delinsCAA ENSP00000518161.1:n.*194_*196delinsCAA
ENST00000688158.2:n.1900_1902delinsCAA
ENST00000688922.2:c.*995_*997delinsCAA ENSP00000508742.2:n.*995_*997delinsCAA
ENST00000700021.1:c.1120_1122delinsCAA ENSP00000514757.1:p.Asn374Gln
ENST00000700022.1:c.*504_*506delinsCAA ENSP00000514758.1:n.*504_*506delinsCAA
ENST00000700023.1:n.2323_2325delinsCAA
ENST00000700024.1:n.2557_2559delinsCAA
ENST00000706954.1:c.1165_1167delinsCAA ENSP00000516674.1:p.Asn389Gln
ENST00000706955.1:c.*1200_*1202delinsCAA ENSP00000516675.1:n.*1200_*1202delinsCAA
ENST00000686459.1:c.*751_*753delinsCAA ENSP00000508909.1:n.*751_*753delinsCAA
ENST00000688158.1:c.*1276_*1278delinsCAA ENSP00000509254.1:n.*1276_*1278delinsCAA
ENST00000688308.1:c.1165_1167delinsCAA ENSP00000508752.1:p.Asn389Gln
ENST00000688922.1:c.1086_1088delinsCAA
ENST00000693560.1:c.1684_1686delinsCAA ENSP00000509861.1:p.Asn562Gln
ENST00000371953.8:c.1165_1167delinsCAA MANE Select ENSP00000361021.3:p.Asn389Gln
ENST00000371953.7:c.1165_1167delinsCAA ENSP00000361021.3:p.Asn389Gln
NM_000314.5:c.1165_1167delinsCAA NP_000305.3:p.Asn389Gln
NM_000314.6:c.1165_1167delinsCAA NP_000305.3:p.Asn389Gln
NM_001304717.2:c.1684_1686delinsCAA NP_001291646.2:p.Asn562Gln
NM_001304718.1:c.574_576delinsCAA NP_001291647.1:p.Asn192Gln
XM_006717926.2:c.1120_1122delinsCAA XP_006717989.1:p.Asn374Gln
XM_011539982.1:c.1069_1071delinsCAA XP_011538284.1:p.Asn357Gln
XR_945791.1:n.1735_1737delinsCAA
NM_000314.7:c.1165_1167delinsCAA NP_000305.3:p.Asn389Gln
NM_001304717.5:c.1684_1686delinsCAA NP_001291646.4:p.Asn562Gln
NM_001304718.2:c.574_576delinsCAA NP_001291647.1:p.Asn192Gln
NM_000314.8:c.1165_1167delinsCAA MANE Select NP_000305.3:p.Asn389Gln