Canonical Allele Identifier: CA891839821
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957954_87957955delinsTG , CM000672.2:g.87957954_87957955delinsTG GRCh38
NC_000010.10:g.89717711_89717712delinsTG , CM000672.1:g.89717711_89717712delinsTG GRCh37
NC_000010.9:g.89707691_89707692delinsTG NCBI36
NG_007466.2:g.99516_99517delinsTG , LRG_311:g.99516_99517delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.736_737delinsTG ENSP00000514759.2:p.Pro246Trp
ENST00000710265.1:c.736_737delinsTG ENSP00000518161.1:p.Pro246Trp
ENST00000472832.3:c.736_737delinsTG ENSP00000483066.2:p.Pro246Trp
ENST00000688158.2:n.1471_1472delinsTG
ENST00000688922.2:c.*566_*567delinsTG ENSP00000508742.2:n.*566_*567delinsTG
ENST00000700021.1:c.691_692delinsTG ENSP00000514757.1:p.Pro231Trp
ENST00000700022.1:c.*75_*76delinsTG ENSP00000514758.1:n.*75_*76delinsTG
ENST00000700023.1:n.1894_1895delinsTG
ENST00000700024.1:n.2128_2129delinsTG
ENST00000700025.1:n.1505_1506delinsTG
ENST00000700026.1:n.373_374delinsTG
ENST00000700029.1:c.570_571delinsTG
ENST00000706954.1:c.736_737delinsTG ENSP00000516674.1:p.Pro246Trp
ENST00000706955.1:c.*771_*772delinsTG ENSP00000516675.1:n.*771_*772delinsTG
ENST00000686459.1:c.*322_*323delinsTG ENSP00000508909.1:n.*322_*323delinsTG
ENST00000688158.1:c.*847_*848delinsTG ENSP00000509254.1:n.*847_*848delinsTG
ENST00000688308.1:c.736_737delinsTG ENSP00000508752.1:p.Pro246Trp
ENST00000688922.1:c.657_658delinsTG
ENST00000693560.1:c.1255_1256delinsTG ENSP00000509861.1:p.Pro419Trp
ENST00000371953.8:c.736_737delinsTG MANE Select ENSP00000361021.3:p.Pro246Trp
ENST00000371953.7:c.736_737delinsTG ENSP00000361021.3:p.Pro246Trp
ENST00000472832.2:c.163_164delinsTG ENSP00000483066.1:p.Pro55Trp
NM_000314.5:c.736_737delinsTG NP_000305.3:p.Pro246Trp
NM_000314.6:c.736_737delinsTG NP_000305.3:p.Pro246Trp
NM_001304717.2:c.1255_1256delinsTG NP_001291646.2:p.Pro419Trp
NM_001304718.1:c.145_146delinsTG NP_001291647.1:p.Pro49Trp
XM_006717926.2:c.691_692delinsTG XP_006717989.1:p.Pro231Trp
XM_011539981.1:c.736_737delinsTG XP_011538283.1:p.Pro246Trp
XM_011539982.1:c.640_641delinsTG XP_011538284.1:p.Pro214Trp
XR_945791.1:n.1306_1307delinsTG
NM_000314.7:c.736_737delinsTG NP_000305.3:p.Pro246Trp
NM_001304717.5:c.1255_1256delinsTG NP_001291646.4:p.Pro419Trp
NM_001304718.2:c.145_146delinsTG NP_001291647.1:p.Pro49Trp
NM_000314.8:c.736_737delinsTG MANE Select NP_000305.3:p.Pro246Trp