Canonical Allele Identifier: CA2579926587

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961107_87961109delinsGTT , CM000672.2:g.87961107_87961109delinsGTT	GRCh38
NC_000010.10:g.89720864_89720866delinsGTT , CM000672.1:g.89720864_89720866delinsGTT	GRCh37
NC_000010.9:g.89710844_89710846delinsGTT	NCBI36
NG_007466.2:g.102669_102671delinsGTT , LRG_311:g.102669_102671delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1108_1110delinsGTT	ENSP00000514759.2:p.Pro370Val
ENST00000710265.1:c.1015_1017delinsGTT	ENSP00000518161.1:p.Pro339Val
ENST00000472832.3:c.1015_1017delinsGTT	ENSP00000483066.2:p.Pro339Val
ENST00000688158.2:n.1750_1752delinsGTT
ENST00000688922.2:c.*845_*847delinsGTT	ENSP00000508742.2:n.*845_*847delinsGTT
ENST00000700021.1:c.970_972delinsGTT	ENSP00000514757.1:p.Pro324Val
ENST00000700022.1:c.*354_*356delinsGTT	ENSP00000514758.1:n.*354_*356delinsGTT
ENST00000700023.1:n.2173_2175delinsGTT
ENST00000700024.1:n.2407_2409delinsGTT
ENST00000700025.1:n.1784_1786delinsGTT
ENST00000700026.1:n.652_654delinsGTT
ENST00000706954.1:c.1015_1017delinsGTT	ENSP00000516674.1:p.Pro339Val
ENST00000706955.1:c.*1050_*1052delinsGTT	ENSP00000516675.1:n.*1050_*1052delinsGTT
ENST00000686459.1:c.*601_*603delinsGTT	ENSP00000508909.1:n.*601_*603delinsGTT
ENST00000688158.1:c.*1126_*1128delinsGTT	ENSP00000509254.1:n.*1126_*1128delinsGTT
ENST00000688308.1:c.1015_1017delinsGTT	ENSP00000508752.1:p.Pro339Val
ENST00000688922.1:c.936_938delinsGTT
ENST00000693560.1:c.1534_1536delinsGTT	ENSP00000509861.1:p.Pro512Val
ENST00000371953.8:c.1015_1017delinsGTT MANE Select	ENSP00000361021.3:p.Pro339Val
ENST00000371953.7:c.1015_1017delinsGTT	ENSP00000361021.3:p.Pro339Val
ENST00000472832.2:c.442_444delinsGTT	ENSP00000483066.1:p.Pro148Val
NM_000314.5:c.1015_1017delinsGTT	NP_000305.3:p.Pro339Val
NM_000314.6:c.1015_1017delinsGTT	NP_000305.3:p.Pro339Val
NM_001304717.2:c.1534_1536delinsGTT	NP_001291646.2:p.Pro512Val
NM_001304718.1:c.424_426delinsGTT	NP_001291647.1:p.Pro142Val
XM_006717926.2:c.970_972delinsGTT	XP_006717989.1:p.Pro324Val
XM_011539981.1:c.1015_1017delinsGTT	XP_011538283.1:p.Pro339Val
XM_011539982.1:c.919_921delinsGTT	XP_011538284.1:p.Pro307Val
XR_945791.1:n.1585_1587delinsGTT
NM_000314.7:c.1015_1017delinsGTT	NP_000305.3:p.Pro339Val
NM_001304717.5:c.1534_1536delinsGTT	NP_001291646.4:p.Pro512Val
NM_001304718.2:c.424_426delinsGTT	NP_001291647.1:p.Pro142Val
NM_000314.8:c.1015_1017delinsGTT MANE Select	NP_000305.3:p.Pro339Val