Canonical Allele Identifier: CA891840283

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960921_87960923delinsGTT , CM000672.2:g.87960921_87960923delinsGTT	GRCh38
NC_000010.10:g.89720678_89720680delinsGTT , CM000672.1:g.89720678_89720680delinsGTT	GRCh37
NC_000010.9:g.89710658_89710660delinsGTT	NCBI36
NG_007466.2:g.102483_102485delinsGTT , LRG_311:g.102483_102485delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.922_924delinsGTT	ENSP00000514759.2:p.Thr308Val
ENST00000710265.1:c.829_831delinsGTT	ENSP00000518161.1:p.Thr277Val
ENST00000472832.3:c.829_831delinsGTT	ENSP00000483066.2:p.Thr277Val
ENST00000688158.2:n.1564_1566delinsGTT
ENST00000688922.2:c.*659_*661delinsGTT	ENSP00000508742.2:n.*659_*661delinsGTT
ENST00000700021.1:c.784_786delinsGTT	ENSP00000514757.1:p.Thr262Val
ENST00000700022.1:c.*168_*170delinsGTT	ENSP00000514758.1:n.*168_*170delinsGTT
ENST00000700023.1:n.1987_1989delinsGTT
ENST00000700024.1:n.2221_2223delinsGTT
ENST00000700025.1:n.1598_1600delinsGTT
ENST00000700026.1:n.466_468delinsGTT
ENST00000700029.1:c.756_758delinsGTT
ENST00000706954.1:c.829_831delinsGTT	ENSP00000516674.1:p.Thr277Val
ENST00000706955.1:c.*864_*866delinsGTT	ENSP00000516675.1:n.*864_*866delinsGTT
ENST00000686459.1:c.*415_*417delinsGTT	ENSP00000508909.1:n.*415_*417delinsGTT
ENST00000688158.1:c.*940_*942delinsGTT	ENSP00000509254.1:n.*940_*942delinsGTT
ENST00000688308.1:c.829_831delinsGTT	ENSP00000508752.1:p.Thr277Val
ENST00000688922.1:c.750_752delinsGTT
ENST00000693560.1:c.1348_1350delinsGTT	ENSP00000509861.1:p.Thr450Val
ENST00000371953.8:c.829_831delinsGTT MANE Select	ENSP00000361021.3:p.Thr277Val
ENST00000371953.7:c.829_831delinsGTT	ENSP00000361021.3:p.Thr277Val
ENST00000472832.2:c.256_258delinsGTT	ENSP00000483066.1:p.Thr86Val
NM_000314.5:c.829_831delinsGTT	NP_000305.3:p.Thr277Val
NM_000314.6:c.829_831delinsGTT	NP_000305.3:p.Thr277Val
NM_001304717.2:c.1348_1350delinsGTT	NP_001291646.2:p.Thr450Val
NM_001304718.1:c.238_240delinsGTT	NP_001291647.1:p.Thr80Val
XM_006717926.2:c.784_786delinsGTT	XP_006717989.1:p.Thr262Val
XM_011539981.1:c.829_831delinsGTT	XP_011538283.1:p.Thr277Val
XM_011539982.1:c.733_735delinsGTT	XP_011538284.1:p.Thr245Val
XR_945791.1:n.1399_1401delinsGTT
NM_000314.7:c.829_831delinsGTT	NP_000305.3:p.Thr277Val
NM_001304717.5:c.1348_1350delinsGTT	NP_001291646.4:p.Thr450Val
NM_001304718.2:c.238_240delinsGTT	NP_001291647.1:p.Thr80Val
NM_000314.8:c.829_831delinsGTT MANE Select	NP_000305.3:p.Thr277Val