Canonical Allele Identifier: CA891834977

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960945_87960947delinsTGT , CM000672.2:g.87960945_87960947delinsTGT	GRCh38
NC_000010.10:g.89720702_89720704delinsTGT , CM000672.1:g.89720702_89720704delinsTGT	GRCh37
NC_000010.9:g.89710682_89710684delinsTGT	NCBI36
NG_007466.2:g.102507_102509delinsTGT , LRG_311:g.102507_102509delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.946_948delinsTGT	ENSP00000514759.2:p.Glu316Cys
ENST00000710265.1:c.853_855delinsTGT	ENSP00000518161.1:p.Glu285Cys
ENST00000472832.3:c.853_855delinsTGT	ENSP00000483066.2:p.Glu285Cys
ENST00000688158.2:n.1588_1590delinsTGT
ENST00000688922.2:c.*683_*685delinsTGT	ENSP00000508742.2:n.*683_*685delinsTGT
ENST00000700021.1:c.808_810delinsTGT	ENSP00000514757.1:p.Glu270Cys
ENST00000700022.1:c.*192_*194delinsTGT	ENSP00000514758.1:n.*192_*194delinsTGT
ENST00000700023.1:n.2011_2013delinsTGT
ENST00000700024.1:n.2245_2247delinsTGT
ENST00000700025.1:n.1622_1624delinsTGT
ENST00000700026.1:n.490_492delinsTGT
ENST00000700029.1:c.780_782delinsTGT
ENST00000706954.1:c.853_855delinsTGT	ENSP00000516674.1:p.Glu285Cys
ENST00000706955.1:c.*888_*890delinsTGT	ENSP00000516675.1:n.*888_*890delinsTGT
ENST00000686459.1:c.*439_*441delinsTGT	ENSP00000508909.1:n.*439_*441delinsTGT
ENST00000688158.1:c.*964_*966delinsTGT	ENSP00000509254.1:n.*964_*966delinsTGT
ENST00000688308.1:c.853_855delinsTGT	ENSP00000508752.1:p.Glu285Cys
ENST00000688922.1:c.774_776delinsTGT
ENST00000693560.1:c.1372_1374delinsTGT	ENSP00000509861.1:p.Glu458Cys
ENST00000371953.8:c.853_855delinsTGT MANE Select	ENSP00000361021.3:p.Glu285Cys
ENST00000371953.7:c.853_855delinsTGT	ENSP00000361021.3:p.Glu285Cys
ENST00000472832.2:c.280_282delinsTGT	ENSP00000483066.1:p.Glu94Cys
NM_000314.5:c.853_855delinsTGT	NP_000305.3:p.Glu285Cys
NM_000314.6:c.853_855delinsTGT	NP_000305.3:p.Glu285Cys
NM_001304717.2:c.1372_1374delinsTGT	NP_001291646.2:p.Glu458Cys
NM_001304718.1:c.262_264delinsTGT	NP_001291647.1:p.Glu88Cys
XM_006717926.2:c.808_810delinsTGT	XP_006717989.1:p.Glu270Cys
XM_011539981.1:c.853_855delinsTGT	XP_011538283.1:p.Glu285Cys
XM_011539982.1:c.757_759delinsTGT	XP_011538284.1:p.Glu253Cys
XR_945791.1:n.1423_1425delinsTGT
NM_000314.7:c.853_855delinsTGT	NP_000305.3:p.Glu285Cys
NM_001304717.5:c.1372_1374delinsTGT	NP_001291646.4:p.Glu458Cys
NM_001304718.2:c.262_264delinsTGT	NP_001291647.1:p.Glu88Cys
NM_000314.8:c.853_855delinsTGT MANE Select	NP_000305.3:p.Glu285Cys