Canonical Allele Identifier: CA891835834

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87931071_87931073delinsTCT , CM000672.2:g.87931071_87931073delinsTCT	GRCh38
NC_000010.10:g.89690828_89690830delinsTCT , CM000672.1:g.89690828_89690830delinsTCT	GRCh37
NC_000010.9:g.89680808_89680810delinsTCT	NCBI36
NG_007466.2:g.72633_72635delinsTCT , LRG_311:g.72633_72635delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.235_237delinsTCT	ENSP00000514759.2:p.Ala79Ser
ENST00000710265.1:c.235_237delinsTCT	ENSP00000518161.1:p.Ala79Ser
ENST00000472832.3:c.235_237delinsTCT	ENSP00000483066.2:p.Ala79Ser
ENST00000688158.2:n.970_972delinsTCT
ENST00000688922.2:c.*65_*67delinsTCT	ENSP00000508742.2:n.*65_*67delinsTCT
ENST00000700021.1:c.190_192delinsTCT	ENSP00000514757.1:p.Ala64Ser
ENST00000700022.1:c.235_237delinsTCT	ENSP00000514758.1:p.Ala79Ser
ENST00000700029.1:c.69_71delinsTCT
ENST00000706954.1:c.235_237delinsTCT	ENSP00000516674.1:p.Ala79Ser
ENST00000706955.1:c.*270_*272delinsTCT	ENSP00000516675.1:n.*270_*272delinsTCT
ENST00000686459.1:c.235_237delinsTCT	ENSP00000508909.1:p.Ala79Ser
ENST00000688158.1:c.*346_*348delinsTCT	ENSP00000509254.1:n.*346_*348delinsTCT
ENST00000688308.1:c.235_237delinsTCT	ENSP00000508752.1:p.Ala79Ser
ENST00000688922.1:c.156_158delinsTCT
ENST00000693560.1:c.754_756delinsTCT	ENSP00000509861.1:p.Ala252Ser
ENST00000371953.8:c.235_237delinsTCT MANE Select	ENSP00000361021.3:p.Ala79Ser
ENST00000371953.7:c.235_237delinsTCT	ENSP00000361021.3:p.Ala79Ser
ENST00000498703.1:n.61_63delinsTCT
ENST00000610634.1:c.133_135delinsTCT	ENSP00000477517.1:p.Ala45Ser
NM_000314.5:c.235_237delinsTCT	NP_000305.3:p.Ala79Ser
NM_000314.6:c.235_237delinsTCT	NP_000305.3:p.Ala79Ser
NM_001304717.2:c.754_756delinsTCT	NP_001291646.2:p.Ala252Ser
NM_001304718.1:c.-516_-514delinsTCT	NP_001291647.1:n.-516_-514delinsTCT
XM_006717926.2:c.190_192delinsTCT	XP_006717989.1:p.Ala64Ser
XM_011539981.1:c.235_237delinsTCT	XP_011538283.1:p.Ala79Ser
XM_011539982.1:c.139_141delinsTCT	XP_011538284.1:p.Ala47Ser
XR_945789.1:n.947_949delinsTCT
XR_945790.1:n.947_949delinsTCT
XR_945791.1:n.947_949delinsTCT
NM_000314.7:c.235_237delinsTCT	NP_000305.3:p.Ala79Ser
NM_001304717.5:c.754_756delinsTCT	NP_001291646.4:p.Ala252Ser
NM_001304718.2:c.-516_-514delinsTCT	NP_001291647.1:n.-516_-514delinsTCT
NM_000314.8:c.235_237delinsTCT MANE Select	NP_000305.3:p.Ala79Ser