Canonical Allele Identifier: CA891839472

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957888_87957890delinsTGG , CM000672.2:g.87957888_87957890delinsTGG	GRCh38
NC_000010.10:g.89717645_89717647delinsTGG , CM000672.1:g.89717645_89717647delinsTGG	GRCh37
NC_000010.9:g.89707625_89707627delinsTGG	NCBI36
NG_007466.2:g.99450_99452delinsTGG , LRG_311:g.99450_99452delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.670_672delinsTGG	ENSP00000514759.2:p.Ile224Trp
ENST00000710265.1:c.670_672delinsTGG	ENSP00000518161.1:p.Ile224Trp
ENST00000472832.3:c.670_672delinsTGG	ENSP00000483066.2:p.Ile224Trp
ENST00000688158.2:n.1405_1407delinsTGG
ENST00000688922.2:c.*500_*502delinsTGG	ENSP00000508742.2:n.*500_*502delinsTGG
ENST00000700021.1:c.625_627delinsTGG	ENSP00000514757.1:p.Ile209Trp
ENST00000700022.1:c.*9_*11delinsTGG	ENSP00000514758.1:n.*9_*11delinsTGG
ENST00000700023.1:n.1828_1830delinsTGG
ENST00000700024.1:n.2062_2064delinsTGG
ENST00000700025.1:n.1439_1441delinsTGG
ENST00000700026.1:n.307_309delinsTGG
ENST00000700029.1:c.504_506delinsTGG
ENST00000706954.1:c.670_672delinsTGG	ENSP00000516674.1:p.Ile224Trp
ENST00000706955.1:c.*705_*707delinsTGG	ENSP00000516675.1:n.*705_*707delinsTGG
ENST00000686459.1:c.*256_*258delinsTGG	ENSP00000508909.1:n.*256_*258delinsTGG
ENST00000688158.1:c.*781_*783delinsTGG	ENSP00000509254.1:n.*781_*783delinsTGG
ENST00000688308.1:c.670_672delinsTGG	ENSP00000508752.1:p.Ile224Trp
ENST00000688922.1:c.591_593delinsTGG
ENST00000693560.1:c.1189_1191delinsTGG	ENSP00000509861.1:p.Ile397Trp
ENST00000371953.8:c.670_672delinsTGG MANE Select	ENSP00000361021.3:p.Ile224Trp
ENST00000371953.7:c.670_672delinsTGG	ENSP00000361021.3:p.Ile224Trp
ENST00000472832.2:c.97_99delinsTGG	ENSP00000483066.1:p.Ile33Trp
NM_000314.5:c.670_672delinsTGG	NP_000305.3:p.Ile224Trp
NM_000314.6:c.670_672delinsTGG	NP_000305.3:p.Ile224Trp
NM_001304717.2:c.1189_1191delinsTGG	NP_001291646.2:p.Ile397Trp
NM_001304718.1:c.79_81delinsTGG	NP_001291647.1:p.Ile27Trp
XM_006717926.2:c.625_627delinsTGG	XP_006717989.1:p.Ile209Trp
XM_011539981.1:c.670_672delinsTGG	XP_011538283.1:p.Ile224Trp
XM_011539982.1:c.574_576delinsTGG	XP_011538284.1:p.Ile192Trp
XR_945791.1:n.1240_1242delinsTGG
NM_000314.7:c.670_672delinsTGG	NP_000305.3:p.Ile224Trp
NM_001304717.5:c.1189_1191delinsTGG	NP_001291646.4:p.Ile397Trp
NM_001304718.2:c.79_81delinsTGG	NP_001291647.1:p.Ile27Trp
NM_000314.8:c.670_672delinsTGG MANE Select	NP_000305.3:p.Ile224Trp