Canonical Allele Identifier: CA891835501

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960981_87960983delinsTGG , CM000672.2:g.87960981_87960983delinsTGG	GRCh38
NC_000010.10:g.89720738_89720740delinsTGG , CM000672.1:g.89720738_89720740delinsTGG	GRCh37
NC_000010.9:g.89710718_89710720delinsTGG	NCBI36
NG_007466.2:g.102543_102545delinsTGG , LRG_311:g.102543_102545delinsTGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.982_984delinsTGG	ENSP00000514759.2:p.Asp328Trp
ENST00000710265.1:c.889_891delinsTGG	ENSP00000518161.1:p.Asp297Trp
ENST00000472832.3:c.889_891delinsTGG	ENSP00000483066.2:p.Asp297Trp
ENST00000688158.2:n.1624_1626delinsTGG
ENST00000688922.2:c.*719_*721delinsTGG	ENSP00000508742.2:n.*719_*721delinsTGG
ENST00000700021.1:c.844_846delinsTGG	ENSP00000514757.1:p.Asp282Trp
ENST00000700022.1:c.*228_*230delinsTGG	ENSP00000514758.1:n.*228_*230delinsTGG
ENST00000700023.1:n.2047_2049delinsTGG
ENST00000700024.1:n.2281_2283delinsTGG
ENST00000700025.1:n.1658_1660delinsTGG
ENST00000700026.1:n.526_528delinsTGG
ENST00000706954.1:c.889_891delinsTGG	ENSP00000516674.1:p.Asp297Trp
ENST00000706955.1:c.*924_*926delinsTGG	ENSP00000516675.1:n.*924_*926delinsTGG
ENST00000686459.1:c.*475_*477delinsTGG	ENSP00000508909.1:n.*475_*477delinsTGG
ENST00000688158.1:c.*1000_*1002delinsTGG	ENSP00000509254.1:n.*1000_*1002delinsTGG
ENST00000688308.1:c.889_891delinsTGG	ENSP00000508752.1:p.Asp297Trp
ENST00000688922.1:c.810_812delinsTGG
ENST00000693560.1:c.1408_1410delinsTGG	ENSP00000509861.1:p.Asp470Trp
ENST00000371953.8:c.889_891delinsTGG MANE Select	ENSP00000361021.3:p.Asp297Trp
ENST00000371953.7:c.889_891delinsTGG	ENSP00000361021.3:p.Asp297Trp
ENST00000472832.2:c.316_318delinsTGG	ENSP00000483066.1:p.Asp106Trp
NM_000314.5:c.889_891delinsTGG	NP_000305.3:p.Asp297Trp
NM_000314.6:c.889_891delinsTGG	NP_000305.3:p.Asp297Trp
NM_001304717.2:c.1408_1410delinsTGG	NP_001291646.2:p.Asp470Trp
NM_001304718.1:c.298_300delinsTGG	NP_001291647.1:p.Asp100Trp
XM_006717926.2:c.844_846delinsTGG	XP_006717989.1:p.Asp282Trp
XM_011539981.1:c.889_891delinsTGG	XP_011538283.1:p.Asp297Trp
XM_011539982.1:c.793_795delinsTGG	XP_011538284.1:p.Asp265Trp
XR_945791.1:n.1459_1461delinsTGG
NM_000314.7:c.889_891delinsTGG	NP_000305.3:p.Asp297Trp
NM_001304717.5:c.1408_1410delinsTGG	NP_001291646.4:p.Asp470Trp
NM_001304718.2:c.298_300delinsTGG	NP_001291647.1:p.Asp100Trp
NM_000314.8:c.889_891delinsTGG MANE Select	NP_000305.3:p.Asp297Trp