Canonical Allele Identifier: CA1926156767
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894022_87894024delinsCAG , CM000672.2:g.87894022_87894024delinsCAG GRCh38
NC_000010.10:g.89653779_89653781delinsCAG , CM000672.1:g.89653779_89653781delinsCAG GRCh37
NC_000010.9:g.89643759_89643761delinsCAG NCBI36
NG_007466.2:g.35584_35586delinsCAG , LRG_311:g.35584_35586delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.80-3_80-1delinsCAG ENSP00000514759.2:n.80-3_80-1delinsCAG
ENST00000710265.1:c.80-3_80-1delinsCAG ENSP00000518161.1:n.80-3_80-1delinsCAG
ENST00000472832.3:c.80-3_80-1delinsCAG ENSP00000483066.2:n.80-3_80-1delinsCAG
ENST00000688158.2:n.899+13584_899+13586delinsCAG
ENST00000688922.2:c.80-3_80-1delinsCAG ENSP00000508742.2:n.80-3_80-1delinsCAG
ENST00000700021.1:c.80-3_80-1delinsCAG ENSP00000514757.1:n.80-3_80-1delinsCAG
ENST00000700022.1:c.80-3_80-1delinsCAG ENSP00000514758.1:n.80-3_80-1delinsCAG
ENST00000706954.1:c.80-3_80-1delinsCAG ENSP00000516674.1:n.80-3_80-1delinsCAG
ENST00000706955.1:c.*115-3_*115-1delinsCAG ENSP00000516675.1:n.*115-3_*115-1delinsCAG
ENST00000686459.1:c.80-3_80-1delinsCAG ENSP00000508909.1:n.80-3_80-1delinsCAG
ENST00000688158.1:c.*275+13584_*275+13586delinsCAG ENSP00000509254.1:n.*275+13584_*275+13586delinsCAG
ENST00000688308.1:c.80-3_80-1delinsCAG ENSP00000508752.1:n.80-3_80-1delinsCAG
ENST00000693560.1:c.599-3_599-1delinsCAG ENSP00000509861.1:n.599-3_599-1delinsCAG
ENST00000371953.8:c.80-3_80-1delinsCAG MANE Select ENSP00000361021.3:n.80-3_80-1delinsCAG
ENST00000371953.7:c.80-3_80-1delinsCAG ENSP00000361021.3:n.80-3_80-1delinsCAG
ENST00000462694.1:n.82-3_82-1delinsCAG
ENST00000610634.1:c.-23-3_-23-1delinsCAG ENSP00000477517.1:n.-23-3_-23-1delinsCAG
NM_000314.5:c.80-3_80-1delinsCAG NP_000305.3:n.80-3_80-1delinsCAG
NM_000314.6:c.80-3_80-1delinsCAG NP_000305.3:n.80-3_80-1delinsCAG
NM_001304717.2:c.599-3_599-1delinsCAG NP_001291646.2:n.599-3_599-1delinsCAG
NM_001304718.1:c.-626-3_-626-1delinsCAG NP_001291647.1:n.-626-3_-626-1delinsCAG
XM_006717926.2:c.80-3_80-1delinsCAG XP_006717989.1:n.80-3_80-1delinsCAG
XM_011539981.1:c.80-3_80-1delinsCAG XP_011538283.1:n.80-3_80-1delinsCAG
XM_011539982.1:c.68+13584_68+13586delinsCAG XP_011538284.1:n.68+13584_68+13586delinsCAG
XR_945789.1:n.792-3_792-1delinsCAG
XR_945790.1:n.792-3_792-1delinsCAG
XR_945791.1:n.792-3_792-1delinsCAG
NM_000314.7:c.80-3_80-1delinsCAG NP_000305.3:n.80-3_80-1delinsCAG
NM_001304717.5:c.599-3_599-1delinsCAG NP_001291646.4:n.599-3_599-1delinsCAG
NM_001304718.2:c.-626-3_-626-1delinsCAG NP_001291647.1:n.-626-3_-626-1delinsCAG
NM_000314.8:c.80-3_80-1delinsCAG MANE Select NP_000305.3:n.80-3_80-1delinsCAG