Canonical Allele Identifier: CA891840840
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957975_87957976delinsCC , CM000672.2:g.87957975_87957976delinsCC GRCh38
NC_000010.10:g.89717732_89717733delinsCC , CM000672.1:g.89717732_89717733delinsCC GRCh37
NC_000010.9:g.89707712_89707713delinsCC NCBI36
NG_007466.2:g.99537_99538delinsCC , LRG_311:g.99537_99538delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.757_758delinsCC ENSP00000514759.2:p.Ile253Pro
ENST00000710265.1:c.757_758delinsCC ENSP00000518161.1:p.Ile253Pro
ENST00000472832.3:c.757_758delinsCC ENSP00000483066.2:p.Ile253Pro
ENST00000688158.2:n.1492_1493delinsCC
ENST00000688922.2:c.*587_*588delinsCC ENSP00000508742.2:n.*587_*588delinsCC
ENST00000700021.1:c.712_713delinsCC ENSP00000514757.1:p.Ile238Pro
ENST00000700022.1:c.*96_*97delinsCC ENSP00000514758.1:n.*96_*97delinsCC
ENST00000700023.1:n.1915_1916delinsCC
ENST00000700024.1:n.2149_2150delinsCC
ENST00000700025.1:n.1526_1527delinsCC
ENST00000700026.1:n.394_395delinsCC
ENST00000700029.1:c.591_592delinsCC
ENST00000706954.1:c.757_758delinsCC ENSP00000516674.1:p.Ile253Pro
ENST00000706955.1:c.*792_*793delinsCC ENSP00000516675.1:n.*792_*793delinsCC
ENST00000686459.1:c.*343_*344delinsCC ENSP00000508909.1:n.*343_*344delinsCC
ENST00000688158.1:c.*868_*869delinsCC ENSP00000509254.1:n.*868_*869delinsCC
ENST00000688308.1:c.757_758delinsCC ENSP00000508752.1:p.Ile253Pro
ENST00000688922.1:c.678_679delinsCC
ENST00000693560.1:c.1276_1277delinsCC ENSP00000509861.1:p.Ile426Pro
ENST00000371953.8:c.757_758delinsCC MANE Select ENSP00000361021.3:p.Ile253Pro
ENST00000371953.7:c.757_758delinsCC ENSP00000361021.3:p.Ile253Pro
ENST00000472832.2:c.184_185delinsCC ENSP00000483066.1:p.Ile62Pro
NM_000314.5:c.757_758delinsCC NP_000305.3:p.Ile253Pro
NM_000314.6:c.757_758delinsCC NP_000305.3:p.Ile253Pro
NM_001304717.2:c.1276_1277delinsCC NP_001291646.2:p.Ile426Pro
NM_001304718.1:c.166_167delinsCC NP_001291647.1:p.Ile56Pro
XM_006717926.2:c.712_713delinsCC XP_006717989.1:p.Ile238Pro
XM_011539981.1:c.757_758delinsCC XP_011538283.1:p.Ile253Pro
XM_011539982.1:c.661_662delinsCC XP_011538284.1:p.Ile221Pro
XR_945791.1:n.1327_1328delinsCC
NM_000314.7:c.757_758delinsCC NP_000305.3:p.Ile253Pro
NM_001304717.5:c.1276_1277delinsCC NP_001291646.4:p.Ile426Pro
NM_001304718.2:c.166_167delinsCC NP_001291647.1:p.Ile56Pro
NM_000314.8:c.757_758delinsCC MANE Select NP_000305.3:p.Ile253Pro