Canonical Allele Identifier: CA891835657

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960987_87960989delinsTGG , CM000672.2:g.87960987_87960989delinsTGG	GRCh38
NC_000010.10:g.89720744_89720746delinsTGG , CM000672.1:g.89720744_89720746delinsTGG	GRCh37
NC_000010.9:g.89710724_89710726delinsTGG	NCBI36
NG_007466.2:g.102549_102551delinsTGG , LRG_311:g.102549_102551delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.988_990delinsTGG	ENSP00000514759.2:p.Glu330Trp
ENST00000710265.1:c.895_897delinsTGG	ENSP00000518161.1:p.Glu299Trp
ENST00000472832.3:c.895_897delinsTGG	ENSP00000483066.2:p.Glu299Trp
ENST00000688158.2:n.1630_1632delinsTGG
ENST00000688922.2:c.*725_*727delinsTGG	ENSP00000508742.2:n.*725_*727delinsTGG
ENST00000700021.1:c.850_852delinsTGG	ENSP00000514757.1:p.Glu284Trp
ENST00000700022.1:c.*234_*236delinsTGG	ENSP00000514758.1:n.*234_*236delinsTGG
ENST00000700023.1:n.2053_2055delinsTGG
ENST00000700024.1:n.2287_2289delinsTGG
ENST00000700025.1:n.1664_1666delinsTGG
ENST00000700026.1:n.532_534delinsTGG
ENST00000706954.1:c.895_897delinsTGG	ENSP00000516674.1:p.Glu299Trp
ENST00000706955.1:c.*930_*932delinsTGG	ENSP00000516675.1:n.*930_*932delinsTGG
ENST00000686459.1:c.*481_*483delinsTGG	ENSP00000508909.1:n.*481_*483delinsTGG
ENST00000688158.1:c.*1006_*1008delinsTGG	ENSP00000509254.1:n.*1006_*1008delinsTGG
ENST00000688308.1:c.895_897delinsTGG	ENSP00000508752.1:p.Glu299Trp
ENST00000688922.1:c.816_818delinsTGG
ENST00000693560.1:c.1414_1416delinsTGG	ENSP00000509861.1:p.Glu472Trp
ENST00000371953.8:c.895_897delinsTGG MANE Select	ENSP00000361021.3:p.Glu299Trp
ENST00000371953.7:c.895_897delinsTGG	ENSP00000361021.3:p.Glu299Trp
ENST00000472832.2:c.322_324delinsTGG	ENSP00000483066.1:p.Glu108Trp
NM_000314.5:c.895_897delinsTGG	NP_000305.3:p.Glu299Trp
NM_000314.6:c.895_897delinsTGG	NP_000305.3:p.Glu299Trp
NM_001304717.2:c.1414_1416delinsTGG	NP_001291646.2:p.Glu472Trp
NM_001304718.1:c.304_306delinsTGG	NP_001291647.1:p.Glu102Trp
XM_006717926.2:c.850_852delinsTGG	XP_006717989.1:p.Glu284Trp
XM_011539981.1:c.895_897delinsTGG	XP_011538283.1:p.Glu299Trp
XM_011539982.1:c.799_801delinsTGG	XP_011538284.1:p.Glu267Trp
XR_945791.1:n.1465_1467delinsTGG
NM_000314.7:c.895_897delinsTGG	NP_000305.3:p.Glu299Trp
NM_001304717.5:c.1414_1416delinsTGG	NP_001291646.4:p.Glu472Trp
NM_001304718.2:c.304_306delinsTGG	NP_001291647.1:p.Glu102Trp
NM_000314.8:c.895_897delinsTGG MANE Select	NP_000305.3:p.Glu299Trp