Canonical Allele Identifier: CA645554052
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM36010

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957973_87958005delinsCGAAAG , CM000672.2:g.87957973_87958005delinsCGAAAG GRCh38
NC_000010.10:g.89717730_89717762delinsCGAAAG , CM000672.1:g.89717730_89717762delinsCGAAAG GRCh37
NC_000010.9:g.89707710_89707742delinsCGAAAG NCBI36
NG_007466.2:g.99535_99567delinsCGAAAG , LRG_311:g.99535_99567delinsCGAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.755_787delinsCGAAAG ENSP00000514759.2:p.Asp252_Lys263delinsAlaLysGlu
ENST00000710265.1:c.755_787delinsCGAAAG ENSP00000518161.1:p.Asp252_Lys263delinsAlaLysGlu
ENST00000472832.3:c.755_787delinsCGAAAG ENSP00000483066.2:p.Asp252_Lys263delinsAlaLysGlu
ENST00000688158.2:n.1490_1522delinsCGAAAG
ENST00000688922.2:c.*585_*617delinsCGAAAG ENSP00000508742.2:n.*585_*617delinsCGAAAG
ENST00000700021.1:c.710_742delinsCGAAAG ENSP00000514757.1:p.Asp237_Lys248delinsAlaLysGlu
ENST00000700022.1:c.*94_*126delinsCGAAAG ENSP00000514758.1:n.*94_*126delinsCGAAAG
ENST00000700023.1:n.1913_1945delinsCGAAAG
ENST00000700024.1:n.2147_2179delinsCGAAAG
ENST00000700025.1:n.1524_1556delinsCGAAAG
ENST00000700026.1:n.392_424delinsCGAAAG
ENST00000700029.1:c.589_621delinsCGAAAG
ENST00000706954.1:c.755_787delinsCGAAAG ENSP00000516674.1:p.Asp252_Lys263delinsAlaLysGlu
ENST00000706955.1:c.*790_*822delinsCGAAAG ENSP00000516675.1:n.*790_*822delinsCGAAAG
ENST00000686459.1:c.*341_*373delinsCGAAAG ENSP00000508909.1:n.*341_*373delinsCGAAAG
ENST00000688158.1:c.*866_*898delinsCGAAAG ENSP00000509254.1:n.*866_*898delinsCGAAAG
ENST00000688308.1:c.755_787delinsCGAAAG ENSP00000508752.1:p.Asp252_Lys263delinsAlaLysGlu
ENST00000688922.1:c.676_708delinsCGAAAG
ENST00000693560.1:c.1274_1306delinsCGAAAG ENSP00000509861.1:p.Asp425_Lys436delinsAlaLysGlu
ENST00000371953.8:c.755_787delinsCGAAAG MANE Select ENSP00000361021.3:p.Asp252_Lys263delinsAlaLysGlu
ENST00000371953.7:c.755_787delinsCGAAAG ENSP00000361021.3:p.Asp252_Lys263delinsAlaLysGlu
ENST00000472832.2:c.182_214delinsCGAAAG ENSP00000483066.1:p.Asp61_Lys72delinsAlaLysGlu
NM_000314.5:c.755_787delinsCGAAAG NP_000305.3:p.Asp252_Lys263delinsAlaLysGlu
NM_000314.6:c.755_787delinsCGAAAG NP_000305.3:p.Asp252_Lys263delinsAlaLysGlu
NM_001304717.2:c.1274_1306delinsCGAAAG NP_001291646.2:p.Asp425_Lys436delinsAlaLysGlu
NM_001304718.1:c.164_196delinsCGAAAG NP_001291647.1:p.Asp55_Lys66delinsAlaLysGlu
XM_006717926.2:c.710_742delinsCGAAAG XP_006717989.1:p.Asp237_Lys248delinsAlaLysGlu
XM_011539981.1:c.755_787delinsCGAAAG XP_011538283.1:p.Asp252_Lys263delinsAlaLysGlu
XM_011539982.1:c.659_691delinsCGAAAG XP_011538284.1:p.Asp220_Lys231delinsAlaLysGlu
XR_945791.1:n.1325_1357delinsCGAAAG
NM_000314.7:c.755_787delinsCGAAAG NP_000305.3:p.Asp252_Lys263delinsAlaLysGlu
NM_001304717.5:c.1274_1306delinsCGAAAG NP_001291646.4:p.Asp425_Lys436delinsAlaLysGlu
NM_001304718.2:c.164_196delinsCGAAAG NP_001291647.1:p.Asp55_Lys66delinsAlaLysGlu
NM_000314.8:c.755_787delinsCGAAAG MANE Select NP_000305.3:p.Asp252_Lys263delinsAlaLysGlu