Canonical Allele Identifier: CA891834750

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960930_87960932delinsTGG , CM000672.2:g.87960930_87960932delinsTGG	GRCh38
NC_000010.10:g.89720687_89720689delinsTGG , CM000672.1:g.89720687_89720689delinsTGG	GRCh37
NC_000010.9:g.89710667_89710669delinsTGG	NCBI36
NG_007466.2:g.102492_102494delinsTGG , LRG_311:g.102492_102494delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.931_933delinsTGG	ENSP00000514759.2:p.Ile311Trp
ENST00000710265.1:c.838_840delinsTGG	ENSP00000518161.1:p.Ile280Trp
ENST00000472832.3:c.838_840delinsTGG	ENSP00000483066.2:p.Ile280Trp
ENST00000688158.2:n.1573_1575delinsTGG
ENST00000688922.2:c.*668_*670delinsTGG	ENSP00000508742.2:n.*668_*670delinsTGG
ENST00000700021.1:c.793_795delinsTGG	ENSP00000514757.1:p.Ile265Trp
ENST00000700022.1:c.*177_*179delinsTGG	ENSP00000514758.1:n.*177_*179delinsTGG
ENST00000700023.1:n.1996_1998delinsTGG
ENST00000700024.1:n.2230_2232delinsTGG
ENST00000700025.1:n.1607_1609delinsTGG
ENST00000700026.1:n.475_477delinsTGG
ENST00000700029.1:c.765_767delinsTGG
ENST00000706954.1:c.838_840delinsTGG	ENSP00000516674.1:p.Ile280Trp
ENST00000706955.1:c.*873_*875delinsTGG	ENSP00000516675.1:n.*873_*875delinsTGG
ENST00000686459.1:c.*424_*426delinsTGG	ENSP00000508909.1:n.*424_*426delinsTGG
ENST00000688158.1:c.*949_*951delinsTGG	ENSP00000509254.1:n.*949_*951delinsTGG
ENST00000688308.1:c.838_840delinsTGG	ENSP00000508752.1:p.Ile280Trp
ENST00000688922.1:c.759_761delinsTGG
ENST00000693560.1:c.1357_1359delinsTGG	ENSP00000509861.1:p.Ile453Trp
ENST00000371953.8:c.838_840delinsTGG MANE Select	ENSP00000361021.3:p.Ile280Trp
ENST00000371953.7:c.838_840delinsTGG	ENSP00000361021.3:p.Ile280Trp
ENST00000472832.2:c.265_267delinsTGG	ENSP00000483066.1:p.Ile89Trp
NM_000314.5:c.838_840delinsTGG	NP_000305.3:p.Ile280Trp
NM_000314.6:c.838_840delinsTGG	NP_000305.3:p.Ile280Trp
NM_001304717.2:c.1357_1359delinsTGG	NP_001291646.2:p.Ile453Trp
NM_001304718.1:c.247_249delinsTGG	NP_001291647.1:p.Ile83Trp
XM_006717926.2:c.793_795delinsTGG	XP_006717989.1:p.Ile265Trp
XM_011539981.1:c.838_840delinsTGG	XP_011538283.1:p.Ile280Trp
XM_011539982.1:c.742_744delinsTGG	XP_011538284.1:p.Ile248Trp
XR_945791.1:n.1408_1410delinsTGG
NM_000314.7:c.838_840delinsTGG	NP_000305.3:p.Ile280Trp
NM_001304717.5:c.1357_1359delinsTGG	NP_001291646.4:p.Ile453Trp
NM_001304718.2:c.247_249delinsTGG	NP_001291647.1:p.Ile83Trp
NM_000314.8:c.838_840delinsTGG MANE Select	NP_000305.3:p.Ile280Trp