Canonical Allele Identifier: CA2579926377

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965464_87965466delinsTGT , CM000672.2:g.87965464_87965466delinsTGT	GRCh38
NC_000010.10:g.89725221_89725223delinsTGT , CM000672.1:g.89725221_89725223delinsTGT	GRCh37
NC_000010.9:g.89715201_89715203delinsTGT	NCBI36
NG_007466.2:g.107026_107028delinsTGT , LRG_311:g.107026_107028delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1297_1299delinsTGT	ENSP00000514759.2:p.Lys433Cys
ENST00000710265.1:c.*233_*235delinsTGT	ENSP00000518161.1:n.*233_*235delinsTGT
ENST00000688158.2:n.1939_1941delinsTGT
ENST00000688922.2:c.*1034_*1036delinsTGT	ENSP00000508742.2:n.*1034_*1036delinsTGT
ENST00000700021.1:c.1159_1161delinsTGT	ENSP00000514757.1:p.Lys387Cys
ENST00000700022.1:c.*543_*545delinsTGT	ENSP00000514758.1:n.*543_*545delinsTGT
ENST00000700023.1:n.2362_2364delinsTGT
ENST00000700024.1:n.2596_2598delinsTGT
ENST00000706954.1:c.1204_1206delinsTGT	ENSP00000516674.1:p.Lys402Cys
ENST00000706955.1:c.*1239_*1241delinsTGT	ENSP00000516675.1:n.*1239_*1241delinsTGT
ENST00000686459.1:c.*790_*792delinsTGT	ENSP00000508909.1:n.*790_*792delinsTGT
ENST00000688158.1:c.*1315_*1317delinsTGT	ENSP00000509254.1:n.*1315_*1317delinsTGT
ENST00000688308.1:c.1204_1206delinsTGT	ENSP00000508752.1:p.Lys402Cys
ENST00000688922.1:c.1125_1127delinsTGT
ENST00000693560.1:c.1723_1725delinsTGT	ENSP00000509861.1:p.Lys575Cys
ENST00000371953.8:c.1204_1206delinsTGT MANE Select	ENSP00000361021.3:p.Lys402Cys
ENST00000371953.7:c.1204_1206delinsTGT	ENSP00000361021.3:p.Lys402Cys
NM_000314.5:c.1204_1206delinsTGT	NP_000305.3:p.Lys402Cys
NM_000314.6:c.1204_1206delinsTGT	NP_000305.3:p.Lys402Cys
NM_001304717.2:c.1723_1725delinsTGT	NP_001291646.2:p.Lys575Cys
NM_001304718.1:c.613_615delinsTGT	NP_001291647.1:p.Lys205Cys
XM_006717926.2:c.1159_1161delinsTGT	XP_006717989.1:p.Lys387Cys
XM_011539982.1:c.1108_1110delinsTGT	XP_011538284.1:p.Lys370Cys
XR_945791.1:n.1774_1776delinsTGT
NM_000314.7:c.1204_1206delinsTGT	NP_000305.3:p.Lys402Cys
NM_001304717.5:c.1723_1725delinsTGT	NP_001291646.4:p.Lys575Cys
NM_001304718.2:c.613_615delinsTGT	NP_001291647.1:p.Lys205Cys
NM_000314.8:c.1204_1206delinsTGT MANE Select	NP_000305.3:p.Lys402Cys