Canonical Allele Identifier: CA470974075
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961063_87961064insG , CM000672.2:g.87961063_87961064insG GRCh38
NC_000010.10:g.89720820_89720821insG , CM000672.1:g.89720820_89720821insG GRCh37
NC_000010.9:g.89710800_89710801insG NCBI36
NG_007466.2:g.102625_102626insG , LRG_311:g.102625_102626insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1064_1065insG ENSP00000514759.2:p.Asp355GlufsTer3
ENST00000710265.1:c.971_972insG ENSP00000518161.1:p.Asp324GlufsTer3
ENST00000472832.3:c.971_972insG ENSP00000483066.2:p.Asp324GlufsTer3
ENST00000688158.2:n.1706_1707insG
ENST00000688922.2:c.*801_*802insG ENSP00000508742.2:n.*801_*802insG
ENST00000700021.1:c.926_927insG ENSP00000514757.1:p.Asp309GlufsTer3
ENST00000700022.1:c.*310_*311insG ENSP00000514758.1:n.*310_*311insG
ENST00000700023.1:n.2129_2130insG
ENST00000700024.1:n.2363_2364insG
ENST00000700025.1:n.1740_1741insG
ENST00000700026.1:n.608_609insG
ENST00000706954.1:c.971_972insG ENSP00000516674.1:p.Asp324GlufsTer3
ENST00000706955.1:c.*1006_*1007insG ENSP00000516675.1:n.*1006_*1007insG
ENST00000686459.1:c.*557_*558insG ENSP00000508909.1:n.*557_*558insG
ENST00000688158.1:c.*1082_*1083insG ENSP00000509254.1:n.*1082_*1083insG
ENST00000688308.1:c.971_972insG ENSP00000508752.1:p.Asp324GlufsTer3
ENST00000688922.1:c.892_893insG
ENST00000693560.1:c.1490_1491insG ENSP00000509861.1:p.Asp497GlufsTer3
ENST00000371953.8:c.971_972insG MANE Select ENSP00000361021.3:p.Asp324GlufsTer3
ENST00000371953.7:c.971_972insG ENSP00000361021.3:p.Asp324GlufsTer3
ENST00000472832.2:c.398_399insG ENSP00000483066.1:p.Asp133GlufsTer3
NM_000314.5:c.971_972insG NP_000305.3:p.Asp324GlufsTer3
NM_000314.6:c.971_972insG NP_000305.3:p.Asp324GlufsTer3
NM_001304717.2:c.1490_1491insG NP_001291646.2:p.Asp497GlufsTer3
NM_001304718.1:c.380_381insG NP_001291647.1:p.Asp127GlufsTer3
XM_006717926.2:c.926_927insG XP_006717989.1:p.Asp309GlufsTer3
XM_011539981.1:c.971_972insG XP_011538283.1:p.Asp324GlufsTer3
XM_011539982.1:c.875_876insG XP_011538284.1:p.Asp292GlufsTer3
XR_945791.1:n.1541_1542insG
NM_000314.7:c.971_972insG NP_000305.3:p.Asp324GlufsTer3
NM_001304717.5:c.1490_1491insG NP_001291646.4:p.Asp497GlufsTer3
NM_001304718.2:c.380_381insG NP_001291647.1:p.Asp127GlufsTer3
NM_000314.8:c.971_972insG MANE Select NP_000305.3:p.Asp324GlufsTer3