Canonical Allele Identifier: CA2579926652

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961089_87961091delinsTTG , CM000672.2:g.87961089_87961091delinsTTG	GRCh38
NC_000010.10:g.89720846_89720848delinsTTG , CM000672.1:g.89720846_89720848delinsTTG	GRCh37
NC_000010.9:g.89710826_89710828delinsTTG	NCBI36
NG_007466.2:g.102651_102653delinsTTG , LRG_311:g.102651_102653delinsTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1090_1092delinsTTG	ENSP00000514759.2:p.Ala364Leu
ENST00000710265.1:c.997_999delinsTTG	ENSP00000518161.1:p.Ala333Leu
ENST00000472832.3:c.997_999delinsTTG	ENSP00000483066.2:p.Ala333Leu
ENST00000688158.2:n.1732_1734delinsTTG
ENST00000688922.2:c.*827_*829delinsTTG	ENSP00000508742.2:n.*827_*829delinsTTG
ENST00000700021.1:c.952_954delinsTTG	ENSP00000514757.1:p.Ala318Leu
ENST00000700022.1:c.*336_*338delinsTTG	ENSP00000514758.1:n.*336_*338delinsTTG
ENST00000700023.1:n.2155_2157delinsTTG
ENST00000700024.1:n.2389_2391delinsTTG
ENST00000700025.1:n.1766_1768delinsTTG
ENST00000700026.1:n.634_636delinsTTG
ENST00000706954.1:c.997_999delinsTTG	ENSP00000516674.1:p.Ala333Leu
ENST00000706955.1:c.*1032_*1034delinsTTG	ENSP00000516675.1:n.*1032_*1034delinsTTG
ENST00000686459.1:c.*583_*585delinsTTG	ENSP00000508909.1:n.*583_*585delinsTTG
ENST00000688158.1:c.*1108_*1110delinsTTG	ENSP00000509254.1:n.*1108_*1110delinsTTG
ENST00000688308.1:c.997_999delinsTTG	ENSP00000508752.1:p.Ala333Leu
ENST00000688922.1:c.918_920delinsTTG
ENST00000693560.1:c.1516_1518delinsTTG	ENSP00000509861.1:p.Ala506Leu
ENST00000371953.8:c.997_999delinsTTG MANE Select	ENSP00000361021.3:p.Ala333Leu
ENST00000371953.7:c.997_999delinsTTG	ENSP00000361021.3:p.Ala333Leu
ENST00000472832.2:c.424_426delinsTTG	ENSP00000483066.1:p.Ala142Leu
NM_000314.5:c.997_999delinsTTG	NP_000305.3:p.Ala333Leu
NM_000314.6:c.997_999delinsTTG	NP_000305.3:p.Ala333Leu
NM_001304717.2:c.1516_1518delinsTTG	NP_001291646.2:p.Ala506Leu
NM_001304718.1:c.406_408delinsTTG	NP_001291647.1:p.Ala136Leu
XM_006717926.2:c.952_954delinsTTG	XP_006717989.1:p.Ala318Leu
XM_011539981.1:c.997_999delinsTTG	XP_011538283.1:p.Ala333Leu
XM_011539982.1:c.901_903delinsTTG	XP_011538284.1:p.Ala301Leu
XR_945791.1:n.1567_1569delinsTTG
NM_000314.7:c.997_999delinsTTG	NP_000305.3:p.Ala333Leu
NM_001304717.5:c.1516_1518delinsTTG	NP_001291646.4:p.Ala506Leu
NM_001304718.2:c.406_408delinsTTG	NP_001291647.1:p.Ala136Leu
NM_000314.8:c.997_999delinsTTG MANE Select	NP_000305.3:p.Ala333Leu