Canonical Allele Identifier: CA891840285

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960922_87960923delinsTG , CM000672.2:g.87960922_87960923delinsTG	GRCh38
NC_000010.10:g.89720679_89720680delinsTG , CM000672.1:g.89720679_89720680delinsTG	GRCh37
NC_000010.9:g.89710659_89710660delinsTG	NCBI36
NG_007466.2:g.102484_102485delinsTG , LRG_311:g.102484_102485delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.923_924delinsTG	ENSP00000514759.2:p.Thr308Met
ENST00000710265.1:c.830_831delinsTG	ENSP00000518161.1:p.Thr277Met
ENST00000472832.3:c.830_831delinsTG	ENSP00000483066.2:p.Thr277Met
ENST00000688158.2:n.1565_1566delinsTG
ENST00000688922.2:c.*660_*661delinsTG	ENSP00000508742.2:n.*660_*661delinsTG
ENST00000700021.1:c.785_786delinsTG	ENSP00000514757.1:p.Thr262Met
ENST00000700022.1:c.*169_*170delinsTG	ENSP00000514758.1:n.*169_*170delinsTG
ENST00000700023.1:n.1988_1989delinsTG
ENST00000700024.1:n.2222_2223delinsTG
ENST00000700025.1:n.1599_1600delinsTG
ENST00000700026.1:n.467_468delinsTG
ENST00000700029.1:c.757_758delinsTG
ENST00000706954.1:c.830_831delinsTG	ENSP00000516674.1:p.Thr277Met
ENST00000706955.1:c.*865_*866delinsTG	ENSP00000516675.1:n.*865_*866delinsTG
ENST00000686459.1:c.*416_*417delinsTG	ENSP00000508909.1:n.*416_*417delinsTG
ENST00000688158.1:c.*941_*942delinsTG	ENSP00000509254.1:n.*941_*942delinsTG
ENST00000688308.1:c.830_831delinsTG	ENSP00000508752.1:p.Thr277Met
ENST00000688922.1:c.751_752delinsTG
ENST00000693560.1:c.1349_1350delinsTG	ENSP00000509861.1:p.Thr450Met
ENST00000371953.8:c.830_831delinsTG MANE Select	ENSP00000361021.3:p.Thr277Met
ENST00000371953.7:c.830_831delinsTG	ENSP00000361021.3:p.Thr277Met
ENST00000472832.2:c.257_258delinsTG	ENSP00000483066.1:p.Thr86Met
NM_000314.5:c.830_831delinsTG	NP_000305.3:p.Thr277Met
NM_000314.6:c.830_831delinsTG	NP_000305.3:p.Thr277Met
NM_001304717.2:c.1349_1350delinsTG	NP_001291646.2:p.Thr450Met
NM_001304718.1:c.239_240delinsTG	NP_001291647.1:p.Thr80Met
XM_006717926.2:c.785_786delinsTG	XP_006717989.1:p.Thr262Met
XM_011539981.1:c.830_831delinsTG	XP_011538283.1:p.Thr277Met
XM_011539982.1:c.734_735delinsTG	XP_011538284.1:p.Thr245Met
XR_945791.1:n.1400_1401delinsTG
NM_000314.7:c.830_831delinsTG	NP_000305.3:p.Thr277Met
NM_001304717.5:c.1349_1350delinsTG	NP_001291646.4:p.Thr450Met
NM_001304718.2:c.239_240delinsTG	NP_001291647.1:p.Thr80Met
NM_000314.8:c.830_831delinsTG MANE Select	NP_000305.3:p.Thr277Met