Canonical Allele Identifier: CA2695200881
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 2674310
ClinVar RCV Id: RCV003452506

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957950_87957951insGG , CM000672.2:g.87957950_87957951insGG GRCh38
NC_000010.10:g.89717707_89717708insGG , CM000672.1:g.89717707_89717708insGG GRCh37
NC_000010.9:g.89707687_89707688insGG NCBI36
NG_007466.2:g.99512_99513insGG , LRG_311:g.99512_99513insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.732_733insGG ENSP00000514759.2:p.Gln245GlyfsTer12
ENST00000710265.1:c.732_733insGG ENSP00000518161.1:p.Gln245GlyfsTer12
ENST00000472832.3:c.732_733insGG ENSP00000483066.2:p.Gln245GlyfsTer12
ENST00000688158.2:n.1467_1468insGG
ENST00000688922.2:c.*562_*563insGG ENSP00000508742.2:n.*562_*563insGG
ENST00000700021.1:c.687_688insGG ENSP00000514757.1:p.Gln230GlyfsTer12
ENST00000700022.1:c.*71_*72insGG ENSP00000514758.1:n.*71_*72insGG
ENST00000700023.1:n.1890_1891insGG
ENST00000700024.1:n.2124_2125insGG
ENST00000700025.1:n.1501_1502insGG
ENST00000700026.1:n.369_370insGG
ENST00000700029.1:c.566_567insGG
ENST00000706954.1:c.732_733insGG ENSP00000516674.1:p.Gln245GlyfsTer12
ENST00000706955.1:c.*767_*768insGG ENSP00000516675.1:n.*767_*768insGG
ENST00000686459.1:c.*318_*319insGG ENSP00000508909.1:n.*318_*319insGG
ENST00000688158.1:c.*843_*844insGG ENSP00000509254.1:n.*843_*844insGG
ENST00000688308.1:c.732_733insGG ENSP00000508752.1:p.Gln245GlyfsTer12
ENST00000688922.1:c.653_654insGG
ENST00000693560.1:c.1251_1252insGG ENSP00000509861.1:p.Gln418GlyfsTer12
ENST00000371953.8:c.732_733insGG MANE Select ENSP00000361021.3:p.Gln245GlyfsTer12
ENST00000371953.7:c.732_733insGG ENSP00000361021.3:p.Gln245GlyfsTer12
ENST00000472832.2:c.159_160insGG ENSP00000483066.1:p.Gln54GlyfsTer12
NM_000314.5:c.732_733insGG NP_000305.3:p.Gln245GlyfsTer12
NM_000314.6:c.732_733insGG NP_000305.3:p.Gln245GlyfsTer12
NM_001304717.2:c.1251_1252insGG NP_001291646.2:p.Gln418GlyfsTer12
NM_001304718.1:c.141_142insGG NP_001291647.1:p.Gln48GlyfsTer12
XM_006717926.2:c.687_688insGG XP_006717989.1:p.Gln230GlyfsTer12
XM_011539981.1:c.732_733insGG XP_011538283.1:p.Gln245GlyfsTer12
XM_011539982.1:c.636_637insGG XP_011538284.1:p.Gln213GlyfsTer12
XR_945791.1:n.1302_1303insGG
NM_000314.7:c.732_733insGG NP_000305.3:p.Gln245GlyfsTer12
NM_001304717.5:c.1251_1252insGG NP_001291646.4:p.Gln418GlyfsTer12
NM_001304718.2:c.141_142insGG NP_001291647.1:p.Gln48GlyfsTer12
NM_000314.8:c.732_733insGG MANE Select NP_000305.3:p.Gln245GlyfsTer12