Canonical Allele Identifier: CA2579926764

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958014_87958016delinsTGG , CM000672.2:g.87958014_87958016delinsTGG	GRCh38
NC_000010.10:g.89717771_89717773delinsTGG , CM000672.1:g.89717771_89717773delinsTGG	GRCh37
NC_000010.9:g.89707751_89707753delinsTGG	NCBI36
NG_007466.2:g.99576_99578delinsTGG , LRG_311:g.99576_99578delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.796_798delinsTGG	ENSP00000514759.2:p.Lys266Trp
ENST00000710265.1:c.796_798delinsTGG	ENSP00000518161.1:p.Lys266Trp
ENST00000472832.3:c.796_798delinsTGG	ENSP00000483066.2:p.Lys266Trp
ENST00000688158.2:n.1531_1533delinsTGG
ENST00000688922.2:c.*626_*628delinsTGG	ENSP00000508742.2:n.*626_*628delinsTGG
ENST00000700021.1:c.751_753delinsTGG	ENSP00000514757.1:p.Lys251Trp
ENST00000700022.1:c.*135_*137delinsTGG	ENSP00000514758.1:n.*135_*137delinsTGG
ENST00000700023.1:n.1954_1956delinsTGG
ENST00000700024.1:n.2188_2190delinsTGG
ENST00000700025.1:n.1565_1567delinsTGG
ENST00000700026.1:n.433_435delinsTGG
ENST00000700029.1:c.630_632delinsTGG
ENST00000706954.1:c.796_798delinsTGG	ENSP00000516674.1:p.Lys266Trp
ENST00000706955.1:c.*831_*833delinsTGG	ENSP00000516675.1:n.*831_*833delinsTGG
ENST00000686459.1:c.*382_*384delinsTGG	ENSP00000508909.1:n.*382_*384delinsTGG
ENST00000688158.1:c.*907_*909delinsTGG	ENSP00000509254.1:n.*907_*909delinsTGG
ENST00000688308.1:c.796_798delinsTGG	ENSP00000508752.1:p.Lys266Trp
ENST00000688922.1:c.717_719delinsTGG
ENST00000693560.1:c.1315_1317delinsTGG	ENSP00000509861.1:p.Lys439Trp
ENST00000371953.8:c.796_798delinsTGG MANE Select	ENSP00000361021.3:p.Lys266Trp
ENST00000371953.7:c.796_798delinsTGG	ENSP00000361021.3:p.Lys266Trp
ENST00000472832.2:c.223_225delinsTGG	ENSP00000483066.1:p.Lys75Trp
NM_000314.5:c.796_798delinsTGG	NP_000305.3:p.Lys266Trp
NM_000314.6:c.796_798delinsTGG	NP_000305.3:p.Lys266Trp
NM_001304717.2:c.1315_1317delinsTGG	NP_001291646.2:p.Lys439Trp
NM_001304718.1:c.205_207delinsTGG	NP_001291647.1:p.Lys69Trp
XM_006717926.2:c.751_753delinsTGG	XP_006717989.1:p.Lys251Trp
XM_011539981.1:c.796_798delinsTGG	XP_011538283.1:p.Lys266Trp
XM_011539982.1:c.700_702delinsTGG	XP_011538284.1:p.Lys234Trp
XR_945791.1:n.1366_1368delinsTGG
NM_000314.7:c.796_798delinsTGG	NP_000305.3:p.Lys266Trp
NM_001304717.5:c.1315_1317delinsTGG	NP_001291646.4:p.Lys439Trp
NM_001304718.2:c.205_207delinsTGG	NP_001291647.1:p.Lys69Trp
NM_000314.8:c.796_798delinsTGG MANE Select	NP_000305.3:p.Lys266Trp