Canonical Allele Identifier: CA470669846
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957961dup , CM000672.2:g.87957961dup GRCh38
NC_000010.10:g.89717718dup , CM000672.1:g.89717718dup GRCh37
NC_000010.9:g.89707698dup NCBI36
NG_007466.2:g.99523dup , LRG_311:g.99523dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.743dup ENSP00000514759.2:p.Val249CysfsTer4
ENST00000710265.1:c.743dup ENSP00000518161.1:p.Val249CysfsTer4
ENST00000472832.3:c.743dup ENSP00000483066.2:p.Val249CysfsTer4
ENST00000688158.2:n.1478dup
ENST00000688922.2:c.*573dup ENSP00000508742.2:n.*573dup
ENST00000700021.1:c.698dup ENSP00000514757.1:p.Val234CysfsTer4
ENST00000700022.1:c.*82dup ENSP00000514758.1:n.*82dup
ENST00000700023.1:n.1901dup
ENST00000700024.1:n.2135dup
ENST00000700025.1:n.1512dup
ENST00000700026.1:n.380dup
ENST00000700029.1:c.577dup
ENST00000706954.1:c.743dup ENSP00000516674.1:p.Val249CysfsTer4
ENST00000706955.1:c.*778dup ENSP00000516675.1:n.*778dup
ENST00000686459.1:c.*329dup ENSP00000508909.1:n.*329dup
ENST00000688158.1:c.*854dup ENSP00000509254.1:n.*854dup
ENST00000688308.1:c.743dup ENSP00000508752.1:p.Val249CysfsTer4
ENST00000688922.1:c.664dup
ENST00000693560.1:c.1262dup ENSP00000509861.1:p.Val422CysfsTer4
ENST00000371953.8:c.743dup MANE Select ENSP00000361021.3:p.Val249CysfsTer4
ENST00000371953.7:c.743dup ENSP00000361021.3:p.Val249CysfsTer4
ENST00000472832.2:c.170dup ENSP00000483066.1:p.Val58CysfsTer4
NM_000314.5:c.743dup NP_000305.3:p.Val249CysfsTer4
NM_000314.6:c.743dup NP_000305.3:p.Val249CysfsTer4
NM_001304717.2:c.1262dup NP_001291646.2:p.Val422CysfsTer4
NM_001304718.1:c.152dup NP_001291647.1:p.Val52CysfsTer4
XM_006717926.2:c.698dup XP_006717989.1:p.Val234CysfsTer4
XM_011539981.1:c.743dup XP_011538283.1:p.Val249CysfsTer4
XM_011539982.1:c.647dup XP_011538284.1:p.Val217CysfsTer4
XR_945791.1:n.1313dup
NM_000314.7:c.743dup NP_000305.3:p.Val249CysfsTer4
NM_001304717.5:c.1262dup NP_001291646.4:p.Val422CysfsTer4
NM_001304718.2:c.152dup NP_001291647.1:p.Val52CysfsTer4
NM_000314.8:c.743dup MANE Select NP_000305.3:p.Val249CysfsTer4