Canonical Allele Identifier: CA891840268

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960918_87960920delinsTGG , CM000672.2:g.87960918_87960920delinsTGG	GRCh38
NC_000010.10:g.89720675_89720677delinsTGG , CM000672.1:g.89720675_89720677delinsTGG	GRCh37
NC_000010.9:g.89710655_89710657delinsTGG	NCBI36
NG_007466.2:g.102480_102482delinsTGG , LRG_311:g.102480_102482delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.919_921delinsTGG	ENSP00000514759.2:p.Asn307Trp
ENST00000710265.1:c.826_828delinsTGG	ENSP00000518161.1:p.Asn276Trp
ENST00000472832.3:c.826_828delinsTGG	ENSP00000483066.2:p.Asn276Trp
ENST00000688158.2:n.1561_1563delinsTGG
ENST00000688922.2:c.*656_*658delinsTGG	ENSP00000508742.2:n.*656_*658delinsTGG
ENST00000700021.1:c.781_783delinsTGG	ENSP00000514757.1:p.Asn261Trp
ENST00000700022.1:c.*165_*167delinsTGG	ENSP00000514758.1:n.*165_*167delinsTGG
ENST00000700023.1:n.1984_1986delinsTGG
ENST00000700024.1:n.2218_2220delinsTGG
ENST00000700025.1:n.1595_1597delinsTGG
ENST00000700026.1:n.463_465delinsTGG
ENST00000700029.1:c.753_755delinsTGG
ENST00000706954.1:c.826_828delinsTGG	ENSP00000516674.1:p.Asn276Trp
ENST00000706955.1:c.*861_*863delinsTGG	ENSP00000516675.1:n.*861_*863delinsTGG
ENST00000686459.1:c.*412_*414delinsTGG	ENSP00000508909.1:n.*412_*414delinsTGG
ENST00000688158.1:c.*937_*939delinsTGG	ENSP00000509254.1:n.*937_*939delinsTGG
ENST00000688308.1:c.826_828delinsTGG	ENSP00000508752.1:p.Asn276Trp
ENST00000688922.1:c.747_749delinsTGG
ENST00000693560.1:c.1345_1347delinsTGG	ENSP00000509861.1:p.Asn449Trp
ENST00000371953.8:c.826_828delinsTGG MANE Select	ENSP00000361021.3:p.Asn276Trp
ENST00000371953.7:c.826_828delinsTGG	ENSP00000361021.3:p.Asn276Trp
ENST00000472832.2:c.253_255delinsTGG	ENSP00000483066.1:p.Asn85Trp
NM_000314.5:c.826_828delinsTGG	NP_000305.3:p.Asn276Trp
NM_000314.6:c.826_828delinsTGG	NP_000305.3:p.Asn276Trp
NM_001304717.2:c.1345_1347delinsTGG	NP_001291646.2:p.Asn449Trp
NM_001304718.1:c.235_237delinsTGG	NP_001291647.1:p.Asn79Trp
XM_006717926.2:c.781_783delinsTGG	XP_006717989.1:p.Asn261Trp
XM_011539981.1:c.826_828delinsTGG	XP_011538283.1:p.Asn276Trp
XM_011539982.1:c.730_732delinsTGG	XP_011538284.1:p.Asn244Trp
XR_945791.1:n.1396_1398delinsTGG
NM_000314.7:c.826_828delinsTGG	NP_000305.3:p.Asn276Trp
NM_001304717.5:c.1345_1347delinsTGG	NP_001291646.4:p.Asn449Trp
NM_001304718.2:c.235_237delinsTGG	NP_001291647.1:p.Asn79Trp
NM_000314.8:c.826_828delinsTGG MANE Select	NP_000305.3:p.Asn276Trp