Canonical Allele Identifier: CA891835305

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960970_87960971delinsAT , CM000672.2:g.87960970_87960971delinsAT	GRCh38
NC_000010.10:g.89720727_89720728delinsAT , CM000672.1:g.89720727_89720728delinsAT	GRCh37
NC_000010.9:g.89710707_89710708delinsAT	NCBI36
NG_007466.2:g.102532_102533delinsAT , LRG_311:g.102532_102533delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.971_972delinsAT	ENSP00000514759.2:p.Gly324Asp
ENST00000710265.1:c.878_879delinsAT	ENSP00000518161.1:p.Gly293Asp
ENST00000472832.3:c.878_879delinsAT	ENSP00000483066.2:p.Gly293Asp
ENST00000688158.2:n.1613_1614delinsAT
ENST00000688922.2:c.*708_*709delinsAT	ENSP00000508742.2:n.*708_*709delinsAT
ENST00000700021.1:c.833_834delinsAT	ENSP00000514757.1:p.Gly278Asp
ENST00000700022.1:c.*217_*218delinsAT	ENSP00000514758.1:n.*217_*218delinsAT
ENST00000700023.1:n.2036_2037delinsAT
ENST00000700024.1:n.2270_2271delinsAT
ENST00000700025.1:n.1647_1648delinsAT
ENST00000700026.1:n.515_516delinsAT
ENST00000700029.1:c.805_806delinsAT
ENST00000706954.1:c.878_879delinsAT	ENSP00000516674.1:p.Gly293Asp
ENST00000706955.1:c.*913_*914delinsAT	ENSP00000516675.1:n.*913_*914delinsAT
ENST00000686459.1:c.*464_*465delinsAT	ENSP00000508909.1:n.*464_*465delinsAT
ENST00000688158.1:c.*989_*990delinsAT	ENSP00000509254.1:n.*989_*990delinsAT
ENST00000688308.1:c.878_879delinsAT	ENSP00000508752.1:p.Gly293Asp
ENST00000688922.1:c.799_800delinsAT
ENST00000693560.1:c.1397_1398delinsAT	ENSP00000509861.1:p.Gly466Asp
ENST00000371953.8:c.878_879delinsAT MANE Select	ENSP00000361021.3:p.Gly293Asp
ENST00000371953.7:c.878_879delinsAT	ENSP00000361021.3:p.Gly293Asp
ENST00000472832.2:c.305_306delinsAT	ENSP00000483066.1:p.Gly102Asp
NM_000314.5:c.878_879delinsAT	NP_000305.3:p.Gly293Asp
NM_000314.6:c.878_879delinsAT	NP_000305.3:p.Gly293Asp
NM_001304717.2:c.1397_1398delinsAT	NP_001291646.2:p.Gly466Asp
NM_001304718.1:c.287_288delinsAT	NP_001291647.1:p.Gly96Asp
XM_006717926.2:c.833_834delinsAT	XP_006717989.1:p.Gly278Asp
XM_011539981.1:c.878_879delinsAT	XP_011538283.1:p.Gly293Asp
XM_011539982.1:c.782_783delinsAT	XP_011538284.1:p.Gly261Asp
XR_945791.1:n.1448_1449delinsAT
NM_000314.7:c.878_879delinsAT	NP_000305.3:p.Gly293Asp
NM_001304717.5:c.1397_1398delinsAT	NP_001291646.4:p.Gly466Asp
NM_001304718.2:c.287_288delinsAT	NP_001291647.1:p.Gly96Asp
NM_000314.8:c.878_879delinsAT MANE Select	NP_000305.3:p.Gly293Asp