Canonical Allele Identifier: CA891840092
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958008_87958010delinsCCA , CM000672.2:g.87958008_87958010delinsCCA GRCh38
NC_000010.10:g.89717765_89717767delinsCCA , CM000672.1:g.89717765_89717767delinsCCA GRCh37
NC_000010.9:g.89707745_89707747delinsCCA NCBI36
NG_007466.2:g.99570_99572delinsCCA , LRG_311:g.99570_99572delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.790_792delinsCCA ENSP00000514759.2:p.Met264Pro
ENST00000710265.1:c.790_792delinsCCA ENSP00000518161.1:p.Met264Pro
ENST00000472832.3:c.790_792delinsCCA ENSP00000483066.2:p.Met264Pro
ENST00000688158.2:n.1525_1527delinsCCA
ENST00000688922.2:c.*620_*622delinsCCA ENSP00000508742.2:n.*620_*622delinsCCA
ENST00000700021.1:c.745_747delinsCCA ENSP00000514757.1:p.Met249Pro
ENST00000700022.1:c.*129_*131delinsCCA ENSP00000514758.1:n.*129_*131delinsCCA
ENST00000700023.1:n.1948_1950delinsCCA
ENST00000700024.1:n.2182_2184delinsCCA
ENST00000700025.1:n.1559_1561delinsCCA
ENST00000700026.1:n.427_429delinsCCA
ENST00000700029.1:c.624_626delinsCCA
ENST00000706954.1:c.790_792delinsCCA ENSP00000516674.1:p.Met264Pro
ENST00000706955.1:c.*825_*827delinsCCA ENSP00000516675.1:n.*825_*827delinsCCA
ENST00000686459.1:c.*376_*378delinsCCA ENSP00000508909.1:n.*376_*378delinsCCA
ENST00000688158.1:c.*901_*903delinsCCA ENSP00000509254.1:n.*901_*903delinsCCA
ENST00000688308.1:c.790_792delinsCCA ENSP00000508752.1:p.Met264Pro
ENST00000688922.1:c.711_713delinsCCA
ENST00000693560.1:c.1309_1311delinsCCA ENSP00000509861.1:p.Met437Pro
ENST00000371953.8:c.790_792delinsCCA MANE Select ENSP00000361021.3:p.Met264Pro
ENST00000371953.7:c.790_792delinsCCA ENSP00000361021.3:p.Met264Pro
ENST00000472832.2:c.217_219delinsCCA ENSP00000483066.1:p.Met73Pro
NM_000314.5:c.790_792delinsCCA NP_000305.3:p.Met264Pro
NM_000314.6:c.790_792delinsCCA NP_000305.3:p.Met264Pro
NM_001304717.2:c.1309_1311delinsCCA NP_001291646.2:p.Met437Pro
NM_001304718.1:c.199_201delinsCCA NP_001291647.1:p.Met67Pro
XM_006717926.2:c.745_747delinsCCA XP_006717989.1:p.Met249Pro
XM_011539981.1:c.790_792delinsCCA XP_011538283.1:p.Met264Pro
XM_011539982.1:c.694_696delinsCCA XP_011538284.1:p.Met232Pro
XR_945791.1:n.1360_1362delinsCCA
NM_000314.7:c.790_792delinsCCA NP_000305.3:p.Met264Pro
NM_001304717.5:c.1309_1311delinsCCA NP_001291646.4:p.Met437Pro
NM_001304718.2:c.199_201delinsCCA NP_001291647.1:p.Met67Pro
NM_000314.8:c.790_792delinsCCA MANE Select NP_000305.3:p.Met264Pro