Canonical Allele Identifier: CA891837425

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965347_87965348delinsGT , CM000672.2:g.87965347_87965348delinsGT	GRCh38
NC_000010.10:g.89725104_89725105delinsGT , CM000672.1:g.89725104_89725105delinsGT	GRCh37
NC_000010.9:g.89715084_89715085delinsGT	NCBI36
NG_007466.2:g.106909_106910delinsGT , LRG_311:g.106909_106910delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1180_1181delinsGT	ENSP00000514759.2:p.Thr394Val
ENST00000710265.1:c.*116_*117delinsGT	ENSP00000518161.1:n.*116_*117delinsGT
ENST00000688158.2:n.1822_1823delinsGT
ENST00000688922.2:c.*917_*918delinsGT	ENSP00000508742.2:n.*917_*918delinsGT
ENST00000700021.1:c.1042_1043delinsGT	ENSP00000514757.1:p.Thr348Val
ENST00000700022.1:c.*426_*427delinsGT	ENSP00000514758.1:n.*426_*427delinsGT
ENST00000700023.1:n.2245_2246delinsGT
ENST00000700024.1:n.2479_2480delinsGT
ENST00000706954.1:c.1087_1088delinsGT	ENSP00000516674.1:p.Thr363Val
ENST00000706955.1:c.*1122_*1123delinsGT	ENSP00000516675.1:n.*1122_*1123delinsGT
ENST00000686459.1:c.*673_*674delinsGT	ENSP00000508909.1:n.*673_*674delinsGT
ENST00000688158.1:c.*1198_*1199delinsGT	ENSP00000509254.1:n.*1198_*1199delinsGT
ENST00000688308.1:c.1087_1088delinsGT	ENSP00000508752.1:p.Thr363Val
ENST00000688922.1:c.1008_1009delinsGT
ENST00000693560.1:c.1606_1607delinsGT	ENSP00000509861.1:p.Thr536Val
ENST00000371953.8:c.1087_1088delinsGT MANE Select	ENSP00000361021.3:p.Thr363Val
ENST00000371953.7:c.1087_1088delinsGT	ENSP00000361021.3:p.Thr363Val
NM_000314.5:c.1087_1088delinsGT	NP_000305.3:p.Thr363Val
NM_000314.6:c.1087_1088delinsGT	NP_000305.3:p.Thr363Val
NM_001304717.2:c.1606_1607delinsGT	NP_001291646.2:p.Thr536Val
NM_001304718.1:c.496_497delinsGT	NP_001291647.1:p.Thr166Val
XM_006717926.2:c.1042_1043delinsGT	XP_006717989.1:p.Thr348Val
XM_011539982.1:c.991_992delinsGT	XP_011538284.1:p.Thr331Val
XR_945791.1:n.1657_1658delinsGT
NM_000314.7:c.1087_1088delinsGT	NP_000305.3:p.Thr363Val
NM_001304717.5:c.1606_1607delinsGT	NP_001291646.4:p.Thr536Val
NM_001304718.2:c.496_497delinsGT	NP_001291647.1:p.Thr166Val
NM_000314.8:c.1087_1088delinsGT MANE Select	NP_000305.3:p.Thr363Val