Canonical Allele Identifier: CA891840940
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958002_87958004delinsAAC , CM000672.2:g.87958002_87958004delinsAAC GRCh38
NC_000010.10:g.89717759_89717761delinsAAC , CM000672.1:g.89717759_89717761delinsAAC GRCh37
NC_000010.9:g.89707739_89707741delinsAAC NCBI36
NG_007466.2:g.99564_99566delinsAAC , LRG_311:g.99564_99566delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.784_786delinsAAC ENSP00000514759.2:p.Asn262=
ENST00000710265.1:c.784_786delinsAAC ENSP00000518161.1:p.Asn262=
ENST00000472832.3:c.784_786delinsAAC ENSP00000483066.2:p.Asn262=
ENST00000688158.2:n.1519_1521delinsAAC
ENST00000688922.2:c.*614_*616delinsAAC ENSP00000508742.2:n.*614_*616delinsAAC
ENST00000700021.1:c.739_741delinsAAC ENSP00000514757.1:p.Asn247=
ENST00000700022.1:c.*123_*125delinsAAC ENSP00000514758.1:n.*123_*125delinsAAC
ENST00000700023.1:n.1942_1944delinsAAC
ENST00000700024.1:n.2176_2178delinsAAC
ENST00000700025.1:n.1553_1555delinsAAC
ENST00000700026.1:n.421_423delinsAAC
ENST00000700029.1:c.618_620delinsAAC
ENST00000706954.1:c.784_786delinsAAC ENSP00000516674.1:p.Asn262=
ENST00000706955.1:c.*819_*821delinsAAC ENSP00000516675.1:n.*819_*821delinsAAC
ENST00000686459.1:c.*370_*372delinsAAC ENSP00000508909.1:n.*370_*372delinsAAC
ENST00000688158.1:c.*895_*897delinsAAC ENSP00000509254.1:n.*895_*897delinsAAC
ENST00000688308.1:c.784_786delinsAAC ENSP00000508752.1:p.Asn262=
ENST00000688922.1:c.705_707delinsAAC
ENST00000693560.1:c.1303_1305delinsAAC ENSP00000509861.1:p.Asn435=
ENST00000371953.8:c.784_786delinsAAC MANE Select ENSP00000361021.3:p.Asn262=
ENST00000371953.7:c.784_786delinsAAC ENSP00000361021.3:p.Asn262=
ENST00000472832.2:c.211_213delinsAAC ENSP00000483066.1:p.Asn71=
NM_000314.5:c.784_786delinsAAC NP_000305.3:p.Asn262=
NM_000314.6:c.784_786delinsAAC NP_000305.3:p.Asn262=
NM_001304717.2:c.1303_1305delinsAAC NP_001291646.2:p.Asn435=
NM_001304718.1:c.193_195delinsAAC NP_001291647.1:p.Asn65=
XM_006717926.2:c.739_741delinsAAC XP_006717989.1:p.Asn247=
XM_011539981.1:c.784_786delinsAAC XP_011538283.1:p.Asn262=
XM_011539982.1:c.688_690delinsAAC XP_011538284.1:p.Asn230=
XR_945791.1:n.1354_1356delinsAAC
NM_000314.7:c.784_786delinsAAC NP_000305.3:p.Asn262=
NM_001304717.5:c.1303_1305delinsAAC NP_001291646.4:p.Asn435=
NM_001304718.2:c.193_195delinsAAC NP_001291647.1:p.Asn65=
NM_000314.8:c.784_786delinsAAC MANE Select NP_000305.3:p.Asn262=