Canonical Allele Identifier: CA470670062
Gene: PTEN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.89717770_89717771insG (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958013_87958014insG , CM000672.2:g.87958013_87958014insG GRCh38
NC_000010.10:g.89717770_89717771insG , CM000672.1:g.89717770_89717771insG GRCh37
NC_000010.9:g.89707750_89707751insG NCBI36
NG_007466.2:g.99575_99576insG , LRG_311:g.99575_99576insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.795_796insG ENSP00000514759.2:p.Lys266GlufsTer?
ENST00000710265.1:c.795_796insG ENSP00000518161.1:p.Lys266GlufsTer?
ENST00000472832.3:c.795_796insG ENSP00000483066.2:p.Lys266GlufsTer?
ENST00000688158.2:n.1530_1531insG
ENST00000688922.2:c.*625_*626insG ENSP00000508742.2:n.*625_*626insG
ENST00000700021.1:c.750_751insG ENSP00000514757.1:p.Lys251GlufsTer?
ENST00000700022.1:c.*134_*135insG ENSP00000514758.1:n.*134_*135insG
ENST00000700023.1:n.1953_1954insG
ENST00000700024.1:n.2187_2188insG
ENST00000700025.1:n.1564_1565insG
ENST00000700026.1:n.432_433insG
ENST00000700029.1:c.629_630insG
ENST00000706954.1:c.795_796insG ENSP00000516674.1:p.Lys266GlufsTer?
ENST00000706955.1:c.*830_*831insG ENSP00000516675.1:n.*830_*831insG
ENST00000686459.1:c.*381_*382insG ENSP00000508909.1:n.*381_*382insG
ENST00000688158.1:c.*906_*907insG ENSP00000509254.1:n.*906_*907insG
ENST00000688308.1:c.795_796insG ENSP00000508752.1:p.Lys266GlufsTer?
ENST00000688922.1:c.716_717insG
ENST00000693560.1:c.1314_1315insG ENSP00000509861.1:p.Lys439GlufsTer?
ENST00000371953.8:c.795_796insG MANE Select ENSP00000361021.3:p.Lys266GlufsTer?
ENST00000371953.7:c.795_796insG ENSP00000361021.3:p.Lys266GlufsTer?
ENST00000472832.2:c.222_223insG ENSP00000483066.1:p.Lys75GlufsTer?
NM_000314.5:c.795_796insG NP_000305.3:p.Lys266GlufsTer?
NM_000314.6:c.795_796insG NP_000305.3:p.Lys266GlufsTer?
NM_001304717.2:c.1314_1315insG NP_001291646.2:p.Lys439GlufsTer?
NM_001304718.1:c.204_205insG NP_001291647.1:p.Lys69GlufsTer?
XM_006717926.2:c.750_751insG XP_006717989.1:p.Lys251GlufsTer?
XM_011539981.1:c.795_796insG XP_011538283.1:p.Lys266GlufsTer?
XM_011539982.1:c.699_700insG XP_011538284.1:p.Lys234GlufsTer?
XR_945791.1:n.1365_1366insG
NM_000314.7:c.795_796insG NP_000305.3:p.Lys266GlufsTer?
NM_001304717.5:c.1314_1315insG NP_001291646.4:p.Lys439GlufsTer?
NM_001304718.2:c.204_205insG NP_001291647.1:p.Lys69GlufsTer?
NM_000314.8:c.795_796insG MANE Select NP_000305.3:p.Lys266GlufsTer?
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