Canonical Allele Identifier: CA645554021
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM30558

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957955_87957956insAGGCTCTGGCCCC , CM000672.2:g.87957955_87957956insAGGCTCTGGCCCC GRCh38
NC_000010.10:g.89717712_89717713insAGGCTCTGGCCCC , CM000672.1:g.89717712_89717713insAGGCTCTGGCCCC GRCh37
NC_000010.9:g.89707692_89707693insAGGCTCTGGCCCC NCBI36
NG_007466.2:g.99517_99518insAGGCTCTGGCCCC , LRG_311:g.99517_99518insAGGCTCTGGCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.737_738insAGGCTCTGGCCCC ENSP00000514759.2:p.Leu247GlyfsTer10
ENST00000710265.1:c.737_738insAGGCTCTGGCCCC ENSP00000518161.1:p.Leu247GlyfsTer10
ENST00000472832.3:c.737_738insAGGCTCTGGCCCC ENSP00000483066.2:p.Leu247GlyfsTer10
ENST00000688158.2:n.1472_1473insAGGCTCTGGCCCC
ENST00000688922.2:c.*567_*568insAGGCTCTGGCCCC ENSP00000508742.2:n.*567_*568insAGGCTCTGGCCCC
ENST00000700021.1:c.692_693insAGGCTCTGGCCCC ENSP00000514757.1:p.Leu232GlyfsTer10
ENST00000700022.1:c.*76_*77insAGGCTCTGGCCCC ENSP00000514758.1:n.*76_*77insAGGCTCTGGCCCC
ENST00000700023.1:n.1895_1896insAGGCTCTGGCCCC
ENST00000700024.1:n.2129_2130insAGGCTCTGGCCCC
ENST00000700025.1:n.1506_1507insAGGCTCTGGCCCC
ENST00000700026.1:n.374_375insAGGCTCTGGCCCC
ENST00000700029.1:c.571_572insAGGCTCTGGCCCC
ENST00000706954.1:c.737_738insAGGCTCTGGCCCC ENSP00000516674.1:p.Leu247GlyfsTer10
ENST00000706955.1:c.*772_*773insAGGCTCTGGCCCC ENSP00000516675.1:n.*772_*773insAGGCTCTGGCCCC
ENST00000686459.1:c.*323_*324insAGGCTCTGGCCCC ENSP00000508909.1:n.*323_*324insAGGCTCTGGCCCC
ENST00000688158.1:c.*848_*849insAGGCTCTGGCCCC ENSP00000509254.1:n.*848_*849insAGGCTCTGGCCCC
ENST00000688308.1:c.737_738insAGGCTCTGGCCCC ENSP00000508752.1:p.Leu247GlyfsTer10
ENST00000688922.1:c.658_659insAGGCTCTGGCCCC
ENST00000693560.1:c.1256_1257insAGGCTCTGGCCCC ENSP00000509861.1:p.Leu420GlyfsTer10
ENST00000371953.8:c.737_738insAGGCTCTGGCCCC MANE Select ENSP00000361021.3:p.Leu247GlyfsTer10
ENST00000371953.7:c.737_738insAGGCTCTGGCCCC ENSP00000361021.3:p.Leu247GlyfsTer10
ENST00000472832.2:c.164_165insAGGCTCTGGCCCC ENSP00000483066.1:p.Leu56GlyfsTer10
NM_000314.5:c.737_738insAGGCTCTGGCCCC NP_000305.3:p.Leu247GlyfsTer10
NM_000314.6:c.737_738insAGGCTCTGGCCCC NP_000305.3:p.Leu247GlyfsTer10
NM_001304717.2:c.1256_1257insAGGCTCTGGCCCC NP_001291646.2:p.Leu420GlyfsTer10
NM_001304718.1:c.146_147insAGGCTCTGGCCCC NP_001291647.1:p.Leu50GlyfsTer10
XM_006717926.2:c.692_693insAGGCTCTGGCCCC XP_006717989.1:p.Leu232GlyfsTer10
XM_011539981.1:c.737_738insAGGCTCTGGCCCC XP_011538283.1:p.Leu247GlyfsTer10
XM_011539982.1:c.641_642insAGGCTCTGGCCCC XP_011538284.1:p.Leu215GlyfsTer10
XR_945791.1:n.1307_1308insAGGCTCTGGCCCC
NM_000314.7:c.737_738insAGGCTCTGGCCCC NP_000305.3:p.Leu247GlyfsTer10
NM_001304717.5:c.1256_1257insAGGCTCTGGCCCC NP_001291646.4:p.Leu420GlyfsTer10
NM_001304718.2:c.146_147insAGGCTCTGGCCCC NP_001291647.1:p.Leu50GlyfsTer10
NM_000314.8:c.737_738insAGGCTCTGGCCCC MANE Select NP_000305.3:p.Leu247GlyfsTer10