Canonical Allele Identifier: CA645554068
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM5751170
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958008_87958009insG , CM000672.2:g.87958008_87958009insG GRCh38
NC_000010.10:g.89717765_89717766insG , CM000672.1:g.89717765_89717766insG GRCh37
NC_000010.9:g.89707745_89707746insG NCBI36
NG_007466.2:g.99570_99571insG , LRG_311:g.99570_99571insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.790_791insG ENSP00000514759.2:p.Met264SerfsTer?
ENST00000710265.1:c.790_791insG ENSP00000518161.1:p.Met264SerfsTer?
ENST00000472832.3:c.790_791insG ENSP00000483066.2:p.Met264SerfsTer?
ENST00000688158.2:n.1525_1526insG
ENST00000688922.2:c.*620_*621insG ENSP00000508742.2:n.*620_*621insG
ENST00000700021.1:c.745_746insG ENSP00000514757.1:p.Met249SerfsTer?
ENST00000700022.1:c.*129_*130insG ENSP00000514758.1:n.*129_*130insG
ENST00000700023.1:n.1948_1949insG
ENST00000700024.1:n.2182_2183insG
ENST00000700025.1:n.1559_1560insG
ENST00000700026.1:n.427_428insG
ENST00000700029.1:c.624_625insG
ENST00000706954.1:c.790_791insG ENSP00000516674.1:p.Met264SerfsTer?
ENST00000706955.1:c.*825_*826insG ENSP00000516675.1:n.*825_*826insG
ENST00000686459.1:c.*376_*377insG ENSP00000508909.1:n.*376_*377insG
ENST00000688158.1:c.*901_*902insG ENSP00000509254.1:n.*901_*902insG
ENST00000688308.1:c.790_791insG ENSP00000508752.1:p.Met264SerfsTer?
ENST00000688922.1:c.711_712insG
ENST00000693560.1:c.1309_1310insG ENSP00000509861.1:p.Met437SerfsTer?
ENST00000371953.8:c.790_791insG MANE Select ENSP00000361021.3:p.Met264SerfsTer?
ENST00000371953.7:c.790_791insG ENSP00000361021.3:p.Met264SerfsTer?
ENST00000472832.2:c.217_218insG ENSP00000483066.1:p.Met73SerfsTer?
NM_000314.5:c.790_791insG NP_000305.3:p.Met264SerfsTer?
NM_000314.6:c.790_791insG NP_000305.3:p.Met264SerfsTer?
NM_001304717.2:c.1309_1310insG NP_001291646.2:p.Met437SerfsTer?
NM_001304718.1:c.199_200insG NP_001291647.1:p.Met67SerfsTer?
XM_006717926.2:c.745_746insG XP_006717989.1:p.Met249SerfsTer?
XM_011539981.1:c.790_791insG XP_011538283.1:p.Met264SerfsTer?
XM_011539982.1:c.694_695insG XP_011538284.1:p.Met232SerfsTer?
XR_945791.1:n.1360_1361insG
NM_000314.7:c.790_791insG NP_000305.3:p.Met264SerfsTer?
NM_001304717.5:c.1309_1310insG NP_001291646.4:p.Met437SerfsTer?
NM_001304718.2:c.199_200insG NP_001291647.1:p.Met67SerfsTer?
NM_000314.8:c.790_791insG MANE Select NP_000305.3:p.Met264SerfsTer?
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