Canonical Allele Identifier: CA891837668

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965378_87965379delinsCT , CM000672.2:g.87965378_87965379delinsCT	GRCh38
NC_000010.10:g.89725135_89725136delinsCT , CM000672.1:g.89725135_89725136delinsCT	GRCh37
NC_000010.9:g.89715115_89715116delinsCT	NCBI36
NG_007466.2:g.106940_106941delinsCT , LRG_311:g.106940_106941delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1211_1212delinsCT	ENSP00000514759.2:p.Glu404Ala
ENST00000710265.1:c.*147_*148delinsCT	ENSP00000518161.1:n.*147_*148delinsCT
ENST00000688158.2:n.1853_1854delinsCT
ENST00000688922.2:c.*948_*949delinsCT	ENSP00000508742.2:n.*948_*949delinsCT
ENST00000700021.1:c.1073_1074delinsCT	ENSP00000514757.1:p.Glu358Ala
ENST00000700022.1:c.*457_*458delinsCT	ENSP00000514758.1:n.*457_*458delinsCT
ENST00000700023.1:n.2276_2277delinsCT
ENST00000700024.1:n.2510_2511delinsCT
ENST00000706954.1:c.1118_1119delinsCT	ENSP00000516674.1:p.Glu373Ala
ENST00000706955.1:c.*1153_*1154delinsCT	ENSP00000516675.1:n.*1153_*1154delinsCT
ENST00000686459.1:c.*704_*705delinsCT	ENSP00000508909.1:n.*704_*705delinsCT
ENST00000688158.1:c.*1229_*1230delinsCT	ENSP00000509254.1:n.*1229_*1230delinsCT
ENST00000688308.1:c.1118_1119delinsCT	ENSP00000508752.1:p.Glu373Ala
ENST00000688922.1:c.1039_1040delinsCT
ENST00000693560.1:c.1637_1638delinsCT	ENSP00000509861.1:p.Glu546Ala
ENST00000371953.8:c.1118_1119delinsCT MANE Select	ENSP00000361021.3:p.Glu373Ala
ENST00000371953.7:c.1118_1119delinsCT	ENSP00000361021.3:p.Glu373Ala
NM_000314.5:c.1118_1119delinsCT	NP_000305.3:p.Glu373Ala
NM_000314.6:c.1118_1119delinsCT	NP_000305.3:p.Glu373Ala
NM_001304717.2:c.1637_1638delinsCT	NP_001291646.2:p.Glu546Ala
NM_001304718.1:c.527_528delinsCT	NP_001291647.1:p.Glu176Ala
XM_006717926.2:c.1073_1074delinsCT	XP_006717989.1:p.Glu358Ala
XM_011539982.1:c.1022_1023delinsCT	XP_011538284.1:p.Glu341Ala
XR_945791.1:n.1688_1689delinsCT
NM_000314.7:c.1118_1119delinsCT	NP_000305.3:p.Glu373Ala
NM_001304717.5:c.1637_1638delinsCT	NP_001291646.4:p.Glu546Ala
NM_001304718.2:c.527_528delinsCT	NP_001291647.1:p.Glu176Ala
NM_000314.8:c.1118_1119delinsCT MANE Select	NP_000305.3:p.Glu373Ala