Canonical Allele Identifier: CA377485698
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs878853944

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960969G>C , CM000672.2:g.87960969G>C GRCh38
NC_000010.10:g.89720726G>C , CM000672.1:g.89720726G>C GRCh37
NC_000010.9:g.89710706G>C NCBI36
NG_007466.2:g.102531G>C , LRG_311:g.102531G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.970G>C ENSP00000514759.2:p.Gly324Arg
ENST00000710265.1:c.877G>C ENSP00000518161.1:p.Gly293Arg
ENST00000472832.3:c.877G>C ENSP00000483066.2:p.Gly293Arg
ENST00000688158.2:n.1612G>C
ENST00000688922.2:c.*707G>C ENSP00000508742.2:n.*707G>C
ENST00000700021.1:c.832G>C ENSP00000514757.1:p.Gly278Arg
ENST00000700022.1:c.*216G>C ENSP00000514758.1:n.*216G>C
ENST00000700023.1:n.2035G>C
ENST00000700024.1:n.2269G>C
ENST00000700025.1:n.1646G>C
ENST00000700026.1:n.514G>C
ENST00000700029.1:c.804G>C
ENST00000706954.1:c.877G>C ENSP00000516674.1:p.Gly293Arg
ENST00000706955.1:c.*912G>C ENSP00000516675.1:n.*912G>C
ENST00000686459.1:c.*463G>C ENSP00000508909.1:n.*463G>C
ENST00000688158.1:c.*988G>C ENSP00000509254.1:n.*988G>C
ENST00000688308.1:c.877G>C ENSP00000508752.1:p.Gly293Arg
ENST00000688922.1:c.798G>C
ENST00000693560.1:c.1396G>C ENSP00000509861.1:p.Gly466Arg
ENST00000371953.8:c.877G>C MANE Select ENSP00000361021.3:p.Gly293Arg
ENST00000371953.7:c.877G>C ENSP00000361021.3:p.Gly293Arg
ENST00000472832.2:c.304G>C ENSP00000483066.1:p.Gly102Arg
NM_000314.5:c.877G>C NP_000305.3:p.Gly293Arg
NM_000314.6:c.877G>C NP_000305.3:p.Gly293Arg
NM_001304717.2:c.1396G>C NP_001291646.2:p.Gly466Arg
NM_001304718.1:c.286G>C NP_001291647.1:p.Gly96Arg
XM_006717926.2:c.832G>C XP_006717989.1:p.Gly278Arg
XM_011539981.1:c.877G>C XP_011538283.1:p.Gly293Arg
XM_011539982.1:c.781G>C XP_011538284.1:p.Gly261Arg
XR_945791.1:n.1447G>C
NM_000314.7:c.877G>C NP_000305.3:p.Gly293Arg
NM_001304717.5:c.1396G>C NP_001291646.4:p.Gly466Arg
NM_001304718.2:c.286G>C NP_001291647.1:p.Gly96Arg
NM_000314.8:c.877G>C MANE Select NP_000305.3:p.Gly293Arg