Canonical Allele Identifier: CA645554051
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957971_87957972insCACGTGCG , CM000672.2:g.87957971_87957972insCACGTGCG GRCh38
NC_000010.10:g.89717728_89717729insCACGTGCG , CM000672.1:g.89717728_89717729insCACGTGCG GRCh37
NC_000010.9:g.89707708_89707709insCACGTGCG NCBI36
NG_007466.2:g.99533_99534insCACGTGCG , LRG_311:g.99533_99534insCACGTGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.753_754insCACGTGCG ENSP00000514759.2:p.Asp252HisfsTer7
ENST00000710265.1:c.753_754insCACGTGCG ENSP00000518161.1:p.Asp252HisfsTer7
ENST00000472832.3:c.753_754insCACGTGCG ENSP00000483066.2:p.Asp252HisfsTer7
ENST00000688158.2:n.1488_1489insCACGTGCG
ENST00000688922.2:c.*583_*584insCACGTGCG ENSP00000508742.2:n.*583_*584insCACGTGCG
ENST00000700021.1:c.708_709insCACGTGCG ENSP00000514757.1:p.Asp237HisfsTer7
ENST00000700022.1:c.*92_*93insCACGTGCG ENSP00000514758.1:n.*92_*93insCACGTGCG
ENST00000700023.1:n.1911_1912insCACGTGCG
ENST00000700024.1:n.2145_2146insCACGTGCG
ENST00000700025.1:n.1522_1523insCACGTGCG
ENST00000700026.1:n.390_391insCACGTGCG
ENST00000700029.1:c.587_588insCACGTGCG
ENST00000706954.1:c.753_754insCACGTGCG ENSP00000516674.1:p.Asp252HisfsTer7
ENST00000706955.1:c.*788_*789insCACGTGCG ENSP00000516675.1:n.*788_*789insCACGTGCG
ENST00000686459.1:c.*339_*340insCACGTGCG ENSP00000508909.1:n.*339_*340insCACGTGCG
ENST00000688158.1:c.*864_*865insCACGTGCG ENSP00000509254.1:n.*864_*865insCACGTGCG
ENST00000688308.1:c.753_754insCACGTGCG ENSP00000508752.1:p.Asp252HisfsTer7
ENST00000688922.1:c.674_675insCACGTGCG
ENST00000693560.1:c.1272_1273insCACGTGCG ENSP00000509861.1:p.Asp425HisfsTer7
ENST00000371953.8:c.753_754insCACGTGCG MANE Select ENSP00000361021.3:p.Asp252HisfsTer7
ENST00000371953.7:c.753_754insCACGTGCG ENSP00000361021.3:p.Asp252HisfsTer7
ENST00000472832.2:c.180_181insCACGTGCG ENSP00000483066.1:p.Asp61HisfsTer7
NM_000314.5:c.753_754insCACGTGCG NP_000305.3:p.Asp252HisfsTer7
NM_000314.6:c.753_754insCACGTGCG NP_000305.3:p.Asp252HisfsTer7
NM_001304717.2:c.1272_1273insCACGTGCG NP_001291646.2:p.Asp425HisfsTer7
NM_001304718.1:c.162_163insCACGTGCG NP_001291647.1:p.Asp55HisfsTer7
XM_006717926.2:c.708_709insCACGTGCG XP_006717989.1:p.Asp237HisfsTer7
XM_011539981.1:c.753_754insCACGTGCG XP_011538283.1:p.Asp252HisfsTer7
XM_011539982.1:c.657_658insCACGTGCG XP_011538284.1:p.Asp220HisfsTer7
XR_945791.1:n.1323_1324insCACGTGCG
NM_000314.7:c.753_754insCACGTGCG NP_000305.3:p.Asp252HisfsTer7
NM_001304717.5:c.1272_1273insCACGTGCG NP_001291646.4:p.Asp425HisfsTer7
NM_001304718.2:c.162_163insCACGTGCG NP_001291647.1:p.Asp55HisfsTer7
NM_000314.8:c.753_754insCACGTGCG MANE Select NP_000305.3:p.Asp252HisfsTer7