Canonical Allele Identifier: CA891839827
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957954_87957955delinsAT , CM000672.2:g.87957954_87957955delinsAT GRCh38
NC_000010.10:g.89717711_89717712delinsAT , CM000672.1:g.89717711_89717712delinsAT GRCh37
NC_000010.9:g.89707691_89707692delinsAT NCBI36
NG_007466.2:g.99516_99517delinsAT , LRG_311:g.99516_99517delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.736_737delinsAT ENSP00000514759.2:p.Pro246Met
ENST00000710265.1:c.736_737delinsAT ENSP00000518161.1:p.Pro246Met
ENST00000472832.3:c.736_737delinsAT ENSP00000483066.2:p.Pro246Met
ENST00000688158.2:n.1471_1472delinsAT
ENST00000688922.2:c.*566_*567delinsAT ENSP00000508742.2:n.*566_*567delinsAT
ENST00000700021.1:c.691_692delinsAT ENSP00000514757.1:p.Pro231Met
ENST00000700022.1:c.*75_*76delinsAT ENSP00000514758.1:n.*75_*76delinsAT
ENST00000700023.1:n.1894_1895delinsAT
ENST00000700024.1:n.2128_2129delinsAT
ENST00000700025.1:n.1505_1506delinsAT
ENST00000700026.1:n.373_374delinsAT
ENST00000700029.1:c.570_571delinsAT
ENST00000706954.1:c.736_737delinsAT ENSP00000516674.1:p.Pro246Met
ENST00000706955.1:c.*771_*772delinsAT ENSP00000516675.1:n.*771_*772delinsAT
ENST00000686459.1:c.*322_*323delinsAT ENSP00000508909.1:n.*322_*323delinsAT
ENST00000688158.1:c.*847_*848delinsAT ENSP00000509254.1:n.*847_*848delinsAT
ENST00000688308.1:c.736_737delinsAT ENSP00000508752.1:p.Pro246Met
ENST00000688922.1:c.657_658delinsAT
ENST00000693560.1:c.1255_1256delinsAT ENSP00000509861.1:p.Pro419Met
ENST00000371953.8:c.736_737delinsAT MANE Select ENSP00000361021.3:p.Pro246Met
ENST00000371953.7:c.736_737delinsAT ENSP00000361021.3:p.Pro246Met
ENST00000472832.2:c.163_164delinsAT ENSP00000483066.1:p.Pro55Met
NM_000314.5:c.736_737delinsAT NP_000305.3:p.Pro246Met
NM_000314.6:c.736_737delinsAT NP_000305.3:p.Pro246Met
NM_001304717.2:c.1255_1256delinsAT NP_001291646.2:p.Pro419Met
NM_001304718.1:c.145_146delinsAT NP_001291647.1:p.Pro49Met
XM_006717926.2:c.691_692delinsAT XP_006717989.1:p.Pro231Met
XM_011539981.1:c.736_737delinsAT XP_011538283.1:p.Pro246Met
XM_011539982.1:c.640_641delinsAT XP_011538284.1:p.Pro214Met
XR_945791.1:n.1306_1307delinsAT
NM_000314.7:c.736_737delinsAT NP_000305.3:p.Pro246Met
NM_001304717.5:c.1255_1256delinsAT NP_001291646.4:p.Pro419Met
NM_001304718.2:c.145_146delinsAT NP_001291647.1:p.Pro49Met
NM_000314.8:c.736_737delinsAT MANE Select NP_000305.3:p.Pro246Met