Canonical Allele Identifier: CA891840054
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958000_87958001delinsCA , CM000672.2:g.87958000_87958001delinsCA GRCh38
NC_000010.10:g.89717757_89717758delinsCA , CM000672.1:g.89717757_89717758delinsCA GRCh37
NC_000010.9:g.89707737_89707738delinsCA NCBI36
NG_007466.2:g.99562_99563delinsCA , LRG_311:g.99562_99563delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.782_783delinsCA ENSP00000514759.2:p.Gln261Pro
ENST00000710265.1:c.782_783delinsCA ENSP00000518161.1:p.Gln261Pro
ENST00000472832.3:c.782_783delinsCA ENSP00000483066.2:p.Gln261Pro
ENST00000688158.2:n.1517_1518delinsCA
ENST00000688922.2:c.*612_*613delinsCA ENSP00000508742.2:n.*612_*613delinsCA
ENST00000700021.1:c.737_738delinsCA ENSP00000514757.1:p.Gln246Pro
ENST00000700022.1:c.*121_*122delinsCA ENSP00000514758.1:n.*121_*122delinsCA
ENST00000700023.1:n.1940_1941delinsCA
ENST00000700024.1:n.2174_2175delinsCA
ENST00000700025.1:n.1551_1552delinsCA
ENST00000700026.1:n.419_420delinsCA
ENST00000700029.1:c.616_617delinsCA
ENST00000706954.1:c.782_783delinsCA ENSP00000516674.1:p.Gln261Pro
ENST00000706955.1:c.*817_*818delinsCA ENSP00000516675.1:n.*817_*818delinsCA
ENST00000686459.1:c.*368_*369delinsCA ENSP00000508909.1:n.*368_*369delinsCA
ENST00000688158.1:c.*893_*894delinsCA ENSP00000509254.1:n.*893_*894delinsCA
ENST00000688308.1:c.782_783delinsCA ENSP00000508752.1:p.Gln261Pro
ENST00000688922.1:c.703_704delinsCA
ENST00000693560.1:c.1301_1302delinsCA ENSP00000509861.1:p.Gln434Pro
ENST00000371953.8:c.782_783delinsCA MANE Select ENSP00000361021.3:p.Gln261Pro
ENST00000371953.7:c.782_783delinsCA ENSP00000361021.3:p.Gln261Pro
ENST00000472832.2:c.209_210delinsCA ENSP00000483066.1:p.Gln70Pro
NM_000314.5:c.782_783delinsCA NP_000305.3:p.Gln261Pro
NM_000314.6:c.782_783delinsCA NP_000305.3:p.Gln261Pro
NM_001304717.2:c.1301_1302delinsCA NP_001291646.2:p.Gln434Pro
NM_001304718.1:c.191_192delinsCA NP_001291647.1:p.Gln64Pro
XM_006717926.2:c.737_738delinsCA XP_006717989.1:p.Gln246Pro
XM_011539981.1:c.782_783delinsCA XP_011538283.1:p.Gln261Pro
XM_011539982.1:c.686_687delinsCA XP_011538284.1:p.Gln229Pro
XR_945791.1:n.1352_1353delinsCA
NM_000314.7:c.782_783delinsCA NP_000305.3:p.Gln261Pro
NM_001304717.5:c.1301_1302delinsCA NP_001291646.4:p.Gln434Pro
NM_001304718.2:c.191_192delinsCA NP_001291647.1:p.Gln64Pro
NM_000314.8:c.782_783delinsCA MANE Select NP_000305.3:p.Gln261Pro