Canonical Allele Identifier: CA891837437

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965350_87965351delinsGT , CM000672.2:g.87965350_87965351delinsGT	GRCh38
NC_000010.10:g.89725107_89725108delinsGT , CM000672.1:g.89725107_89725108delinsGT	GRCh37
NC_000010.9:g.89715087_89715088delinsGT	NCBI36
NG_007466.2:g.106912_106913delinsGT , LRG_311:g.106912_106913delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1183_1184delinsGT	ENSP00000514759.2:p.Ser395Val
ENST00000710265.1:c.*119_*120delinsGT	ENSP00000518161.1:n.*119_*120delinsGT
ENST00000688158.2:n.1825_1826delinsGT
ENST00000688922.2:c.*920_*921delinsGT	ENSP00000508742.2:n.*920_*921delinsGT
ENST00000700021.1:c.1045_1046delinsGT	ENSP00000514757.1:p.Ser349Val
ENST00000700022.1:c.*429_*430delinsGT	ENSP00000514758.1:n.*429_*430delinsGT
ENST00000700023.1:n.2248_2249delinsGT
ENST00000700024.1:n.2482_2483delinsGT
ENST00000706954.1:c.1090_1091delinsGT	ENSP00000516674.1:p.Ser364Val
ENST00000706955.1:c.*1125_*1126delinsGT	ENSP00000516675.1:n.*1125_*1126delinsGT
ENST00000686459.1:c.*676_*677delinsGT	ENSP00000508909.1:n.*676_*677delinsGT
ENST00000688158.1:c.*1201_*1202delinsGT	ENSP00000509254.1:n.*1201_*1202delinsGT
ENST00000688308.1:c.1090_1091delinsGT	ENSP00000508752.1:p.Ser364Val
ENST00000688922.1:c.1011_1012delinsGT
ENST00000693560.1:c.1609_1610delinsGT	ENSP00000509861.1:p.Ser537Val
ENST00000371953.8:c.1090_1091delinsGT MANE Select	ENSP00000361021.3:p.Ser364Val
ENST00000371953.7:c.1090_1091delinsGT	ENSP00000361021.3:p.Ser364Val
NM_000314.5:c.1090_1091delinsGT	NP_000305.3:p.Ser364Val
NM_000314.6:c.1090_1091delinsGT	NP_000305.3:p.Ser364Val
NM_001304717.2:c.1609_1610delinsGT	NP_001291646.2:p.Ser537Val
NM_001304718.1:c.499_500delinsGT	NP_001291647.1:p.Ser167Val
XM_006717926.2:c.1045_1046delinsGT	XP_006717989.1:p.Ser349Val
XM_011539982.1:c.994_995delinsGT	XP_011538284.1:p.Ser332Val
XR_945791.1:n.1660_1661delinsGT
NM_000314.7:c.1090_1091delinsGT	NP_000305.3:p.Ser364Val
NM_001304717.5:c.1609_1610delinsGT	NP_001291646.4:p.Ser537Val
NM_001304718.2:c.499_500delinsGT	NP_001291647.1:p.Ser167Val
NM_000314.8:c.1090_1091delinsGT MANE Select	NP_000305.3:p.Ser364Val