Canonical Allele Identifier: CA891838142

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965443_87965445delinsTGG , CM000672.2:g.87965443_87965445delinsTGG	GRCh38
NC_000010.10:g.89725200_89725202delinsTGG , CM000672.1:g.89725200_89725202delinsTGG	GRCh37
NC_000010.9:g.89715180_89715182delinsTGG	NCBI36
NG_007466.2:g.107005_107007delinsTGG , LRG_311:g.107005_107007delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1276_1278delinsTGG	ENSP00000514759.2:p.Asp426Trp
ENST00000710265.1:c.*212_*214delinsTGG	ENSP00000518161.1:n.*212_*214delinsTGG
ENST00000688158.2:n.1918_1920delinsTGG
ENST00000688922.2:c.*1013_*1015delinsTGG	ENSP00000508742.2:n.*1013_*1015delinsTGG
ENST00000700021.1:c.1138_1140delinsTGG	ENSP00000514757.1:p.Asp380Trp
ENST00000700022.1:c.*522_*524delinsTGG	ENSP00000514758.1:n.*522_*524delinsTGG
ENST00000700023.1:n.2341_2343delinsTGG
ENST00000700024.1:n.2575_2577delinsTGG
ENST00000706954.1:c.1183_1185delinsTGG	ENSP00000516674.1:p.Asp395Trp
ENST00000706955.1:c.*1218_*1220delinsTGG	ENSP00000516675.1:n.*1218_*1220delinsTGG
ENST00000686459.1:c.*769_*771delinsTGG	ENSP00000508909.1:n.*769_*771delinsTGG
ENST00000688158.1:c.*1294_*1296delinsTGG	ENSP00000509254.1:n.*1294_*1296delinsTGG
ENST00000688308.1:c.1183_1185delinsTGG	ENSP00000508752.1:p.Asp395Trp
ENST00000688922.1:c.1104_1106delinsTGG
ENST00000693560.1:c.1702_1704delinsTGG	ENSP00000509861.1:p.Asp568Trp
ENST00000371953.8:c.1183_1185delinsTGG MANE Select	ENSP00000361021.3:p.Asp395Trp
ENST00000371953.7:c.1183_1185delinsTGG	ENSP00000361021.3:p.Asp395Trp
NM_000314.5:c.1183_1185delinsTGG	NP_000305.3:p.Asp395Trp
NM_000314.6:c.1183_1185delinsTGG	NP_000305.3:p.Asp395Trp
NM_001304717.2:c.1702_1704delinsTGG	NP_001291646.2:p.Asp568Trp
NM_001304718.1:c.592_594delinsTGG	NP_001291647.1:p.Asp198Trp
XM_006717926.2:c.1138_1140delinsTGG	XP_006717989.1:p.Asp380Trp
XM_011539982.1:c.1087_1089delinsTGG	XP_011538284.1:p.Asp363Trp
XR_945791.1:n.1753_1755delinsTGG
NM_000314.7:c.1183_1185delinsTGG	NP_000305.3:p.Asp395Trp
NM_001304717.5:c.1702_1704delinsTGG	NP_001291646.4:p.Asp568Trp
NM_001304718.2:c.592_594delinsTGG	NP_001291647.1:p.Asp198Trp
NM_000314.8:c.1183_1185delinsTGG MANE Select	NP_000305.3:p.Asp395Trp