Canonical Allele Identifier: CA891841037

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960921_87960922delinsGT , CM000672.2:g.87960921_87960922delinsGT	GRCh38
NC_000010.10:g.89720678_89720679delinsGT , CM000672.1:g.89720678_89720679delinsGT	GRCh37
NC_000010.9:g.89710658_89710659delinsGT	NCBI36
NG_007466.2:g.102483_102484delinsGT , LRG_311:g.102483_102484delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.922_923delinsGT	ENSP00000514759.2:p.Thr308Val
ENST00000710265.1:c.829_830delinsGT	ENSP00000518161.1:p.Thr277Val
ENST00000472832.3:c.829_830delinsGT	ENSP00000483066.2:p.Thr277Val
ENST00000688158.2:n.1564_1565delinsGT
ENST00000688922.2:c.*659_*660delinsGT	ENSP00000508742.2:n.*659_*660delinsGT
ENST00000700021.1:c.784_785delinsGT	ENSP00000514757.1:p.Thr262Val
ENST00000700022.1:c.*168_*169delinsGT	ENSP00000514758.1:n.*168_*169delinsGT
ENST00000700023.1:n.1987_1988delinsGT
ENST00000700024.1:n.2221_2222delinsGT
ENST00000700025.1:n.1598_1599delinsGT
ENST00000700026.1:n.466_467delinsGT
ENST00000700029.1:c.756_757delinsGT
ENST00000706954.1:c.829_830delinsGT	ENSP00000516674.1:p.Thr277Val
ENST00000706955.1:c.*864_*865delinsGT	ENSP00000516675.1:n.*864_*865delinsGT
ENST00000686459.1:c.*415_*416delinsGT	ENSP00000508909.1:n.*415_*416delinsGT
ENST00000688158.1:c.*940_*941delinsGT	ENSP00000509254.1:n.*940_*941delinsGT
ENST00000688308.1:c.829_830delinsGT	ENSP00000508752.1:p.Thr277Val
ENST00000688922.1:c.750_751delinsGT
ENST00000693560.1:c.1348_1349delinsGT	ENSP00000509861.1:p.Thr450Val
ENST00000371953.8:c.829_830delinsGT MANE Select	ENSP00000361021.3:p.Thr277Val
ENST00000371953.7:c.829_830delinsGT	ENSP00000361021.3:p.Thr277Val
ENST00000472832.2:c.256_257delinsGT	ENSP00000483066.1:p.Thr86Val
NM_000314.5:c.829_830delinsGT	NP_000305.3:p.Thr277Val
NM_000314.6:c.829_830delinsGT	NP_000305.3:p.Thr277Val
NM_001304717.2:c.1348_1349delinsGT	NP_001291646.2:p.Thr450Val
NM_001304718.1:c.238_239delinsGT	NP_001291647.1:p.Thr80Val
XM_006717926.2:c.784_785delinsGT	XP_006717989.1:p.Thr262Val
XM_011539981.1:c.829_830delinsGT	XP_011538283.1:p.Thr277Val
XM_011539982.1:c.733_734delinsGT	XP_011538284.1:p.Thr245Val
XR_945791.1:n.1399_1400delinsGT
NM_000314.7:c.829_830delinsGT	NP_000305.3:p.Thr277Val
NM_001304717.5:c.1348_1349delinsGT	NP_001291646.4:p.Thr450Val
NM_001304718.2:c.238_239delinsGT	NP_001291647.1:p.Thr80Val
NM_000314.8:c.829_830delinsGT MANE Select	NP_000305.3:p.Thr277Val