Canonical Allele Identifier: CA645554019
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM30559

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957955_87957956insTGACC , CM000672.2:g.87957955_87957956insTGACC GRCh38
NC_000010.10:g.89717712_89717713insTGACC , CM000672.1:g.89717712_89717713insTGACC GRCh37
NC_000010.9:g.89707692_89707693insTGACC NCBI36
NG_007466.2:g.99517_99518insTGACC , LRG_311:g.99517_99518insTGACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.737_738insTGACC ENSP00000514759.2:p.Leu247AspfsTer11
ENST00000710265.1:c.737_738insTGACC ENSP00000518161.1:p.Leu247AspfsTer11
ENST00000472832.3:c.737_738insTGACC ENSP00000483066.2:p.Leu247AspfsTer11
ENST00000688158.2:n.1472_1473insTGACC
ENST00000688922.2:c.*567_*568insTGACC ENSP00000508742.2:n.*567_*568insTGACC
ENST00000700021.1:c.692_693insTGACC ENSP00000514757.1:p.Leu232AspfsTer11
ENST00000700022.1:c.*76_*77insTGACC ENSP00000514758.1:n.*76_*77insTGACC
ENST00000700023.1:n.1895_1896insTGACC
ENST00000700024.1:n.2129_2130insTGACC
ENST00000700025.1:n.1506_1507insTGACC
ENST00000700026.1:n.374_375insTGACC
ENST00000700029.1:c.571_572insTGACC
ENST00000706954.1:c.737_738insTGACC ENSP00000516674.1:p.Leu247AspfsTer11
ENST00000706955.1:c.*772_*773insTGACC ENSP00000516675.1:n.*772_*773insTGACC
ENST00000686459.1:c.*323_*324insTGACC ENSP00000508909.1:n.*323_*324insTGACC
ENST00000688158.1:c.*848_*849insTGACC ENSP00000509254.1:n.*848_*849insTGACC
ENST00000688308.1:c.737_738insTGACC ENSP00000508752.1:p.Leu247AspfsTer11
ENST00000688922.1:c.658_659insTGACC
ENST00000693560.1:c.1256_1257insTGACC ENSP00000509861.1:p.Leu420AspfsTer11
ENST00000371953.8:c.737_738insTGACC MANE Select ENSP00000361021.3:p.Leu247AspfsTer11
ENST00000371953.7:c.737_738insTGACC ENSP00000361021.3:p.Leu247AspfsTer11
ENST00000472832.2:c.164_165insTGACC ENSP00000483066.1:p.Leu56AspfsTer11
NM_000314.5:c.737_738insTGACC NP_000305.3:p.Leu247AspfsTer11
NM_000314.6:c.737_738insTGACC NP_000305.3:p.Leu247AspfsTer11
NM_001304717.2:c.1256_1257insTGACC NP_001291646.2:p.Leu420AspfsTer11
NM_001304718.1:c.146_147insTGACC NP_001291647.1:p.Leu50AspfsTer11
XM_006717926.2:c.692_693insTGACC XP_006717989.1:p.Leu232AspfsTer11
XM_011539981.1:c.737_738insTGACC XP_011538283.1:p.Leu247AspfsTer11
XM_011539982.1:c.641_642insTGACC XP_011538284.1:p.Leu215AspfsTer11
XR_945791.1:n.1307_1308insTGACC
NM_000314.7:c.737_738insTGACC NP_000305.3:p.Leu247AspfsTer11
NM_001304717.5:c.1256_1257insTGACC NP_001291646.4:p.Leu420AspfsTer11
NM_001304718.2:c.146_147insTGACC NP_001291647.1:p.Leu50AspfsTer11
NM_000314.8:c.737_738insTGACC MANE Select NP_000305.3:p.Leu247AspfsTer11