Canonical Allele Identifier: CA2579926650

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961089_87961091delinsTGG , CM000672.2:g.87961089_87961091delinsTGG	GRCh38
NC_000010.10:g.89720846_89720848delinsTGG , CM000672.1:g.89720846_89720848delinsTGG	GRCh37
NC_000010.9:g.89710826_89710828delinsTGG	NCBI36
NG_007466.2:g.102651_102653delinsTGG , LRG_311:g.102651_102653delinsTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1090_1092delinsTGG	ENSP00000514759.2:p.Ala364Trp
ENST00000710265.1:c.997_999delinsTGG	ENSP00000518161.1:p.Ala333Trp
ENST00000472832.3:c.997_999delinsTGG	ENSP00000483066.2:p.Ala333Trp
ENST00000688158.2:n.1732_1734delinsTGG
ENST00000688922.2:c.*827_*829delinsTGG	ENSP00000508742.2:n.*827_*829delinsTGG
ENST00000700021.1:c.952_954delinsTGG	ENSP00000514757.1:p.Ala318Trp
ENST00000700022.1:c.*336_*338delinsTGG	ENSP00000514758.1:n.*336_*338delinsTGG
ENST00000700023.1:n.2155_2157delinsTGG
ENST00000700024.1:n.2389_2391delinsTGG
ENST00000700025.1:n.1766_1768delinsTGG
ENST00000700026.1:n.634_636delinsTGG
ENST00000706954.1:c.997_999delinsTGG	ENSP00000516674.1:p.Ala333Trp
ENST00000706955.1:c.*1032_*1034delinsTGG	ENSP00000516675.1:n.*1032_*1034delinsTGG
ENST00000686459.1:c.*583_*585delinsTGG	ENSP00000508909.1:n.*583_*585delinsTGG
ENST00000688158.1:c.*1108_*1110delinsTGG	ENSP00000509254.1:n.*1108_*1110delinsTGG
ENST00000688308.1:c.997_999delinsTGG	ENSP00000508752.1:p.Ala333Trp
ENST00000688922.1:c.918_920delinsTGG
ENST00000693560.1:c.1516_1518delinsTGG	ENSP00000509861.1:p.Ala506Trp
ENST00000371953.8:c.997_999delinsTGG MANE Select	ENSP00000361021.3:p.Ala333Trp
ENST00000371953.7:c.997_999delinsTGG	ENSP00000361021.3:p.Ala333Trp
ENST00000472832.2:c.424_426delinsTGG	ENSP00000483066.1:p.Ala142Trp
NM_000314.5:c.997_999delinsTGG	NP_000305.3:p.Ala333Trp
NM_000314.6:c.997_999delinsTGG	NP_000305.3:p.Ala333Trp
NM_001304717.2:c.1516_1518delinsTGG	NP_001291646.2:p.Ala506Trp
NM_001304718.1:c.406_408delinsTGG	NP_001291647.1:p.Ala136Trp
XM_006717926.2:c.952_954delinsTGG	XP_006717989.1:p.Ala318Trp
XM_011539981.1:c.997_999delinsTGG	XP_011538283.1:p.Ala333Trp
XM_011539982.1:c.901_903delinsTGG	XP_011538284.1:p.Ala301Trp
XR_945791.1:n.1567_1569delinsTGG
NM_000314.7:c.997_999delinsTGG	NP_000305.3:p.Ala333Trp
NM_001304717.5:c.1516_1518delinsTGG	NP_001291646.4:p.Ala506Trp
NM_001304718.2:c.406_408delinsTGG	NP_001291647.1:p.Ala136Trp
NM_000314.8:c.997_999delinsTGG MANE Select	NP_000305.3:p.Ala333Trp