Canonical Allele Identifier: CA891837262

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965332_87965333delinsTG , CM000672.2:g.87965332_87965333delinsTG	GRCh38
NC_000010.10:g.89725089_89725090delinsTG , CM000672.1:g.89725089_89725090delinsTG	GRCh37
NC_000010.9:g.89715069_89715070delinsTG	NCBI36
NG_007466.2:g.106894_106895delinsTG , LRG_311:g.106894_106895delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1165_1166delinsTG	ENSP00000514759.2:p.Glu389Trp
ENST00000710265.1:c.*101_*102delinsTG	ENSP00000518161.1:n.*101_*102delinsTG
ENST00000688158.2:n.1807_1808delinsTG
ENST00000688922.2:c.*902_*903delinsTG	ENSP00000508742.2:n.*902_*903delinsTG
ENST00000700021.1:c.1027_1028delinsTG	ENSP00000514757.1:p.Glu343Trp
ENST00000700022.1:c.*411_*412delinsTG	ENSP00000514758.1:n.*411_*412delinsTG
ENST00000700023.1:n.2230_2231delinsTG
ENST00000700024.1:n.2464_2465delinsTG
ENST00000706954.1:c.1072_1073delinsTG	ENSP00000516674.1:p.Glu358Trp
ENST00000706955.1:c.*1107_*1108delinsTG	ENSP00000516675.1:n.*1107_*1108delinsTG
ENST00000686459.1:c.*658_*659delinsTG	ENSP00000508909.1:n.*658_*659delinsTG
ENST00000688158.1:c.*1183_*1184delinsTG	ENSP00000509254.1:n.*1183_*1184delinsTG
ENST00000688308.1:c.1072_1073delinsTG	ENSP00000508752.1:p.Glu358Trp
ENST00000688922.1:c.993_994delinsTG
ENST00000693560.1:c.1591_1592delinsTG	ENSP00000509861.1:p.Glu531Trp
ENST00000371953.8:c.1072_1073delinsTG MANE Select	ENSP00000361021.3:p.Glu358Trp
ENST00000371953.7:c.1072_1073delinsTG	ENSP00000361021.3:p.Glu358Trp
NM_000314.5:c.1072_1073delinsTG	NP_000305.3:p.Glu358Trp
NM_000314.6:c.1072_1073delinsTG	NP_000305.3:p.Glu358Trp
NM_001304717.2:c.1591_1592delinsTG	NP_001291646.2:p.Glu531Trp
NM_001304718.1:c.481_482delinsTG	NP_001291647.1:p.Glu161Trp
XM_006717926.2:c.1027_1028delinsTG	XP_006717989.1:p.Glu343Trp
XM_011539982.1:c.976_977delinsTG	XP_011538284.1:p.Glu326Trp
XR_945791.1:n.1642_1643delinsTG
NM_000314.7:c.1072_1073delinsTG	NP_000305.3:p.Glu358Trp
NM_001304717.5:c.1591_1592delinsTG	NP_001291646.4:p.Glu531Trp
NM_001304718.2:c.481_482delinsTG	NP_001291647.1:p.Glu161Trp
NM_000314.8:c.1072_1073delinsTG MANE Select	NP_000305.3:p.Glu358Trp