Canonical Allele Identifier: CA891841732

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965464_87965466delinsTAT , CM000672.2:g.87965464_87965466delinsTAT	GRCh38
NC_000010.10:g.89725221_89725223delinsTAT , CM000672.1:g.89725221_89725223delinsTAT	GRCh37
NC_000010.9:g.89715201_89715203delinsTAT	NCBI36
NG_007466.2:g.107026_107028delinsTAT , LRG_311:g.107026_107028delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1297_1299delinsTAT	ENSP00000514759.2:p.Lys433Tyr
ENST00000710265.1:c.*233_*235delinsTAT	ENSP00000518161.1:n.*233_*235delinsTAT
ENST00000688158.2:n.1939_1941delinsTAT
ENST00000688922.2:c.*1034_*1036delinsTAT	ENSP00000508742.2:n.*1034_*1036delinsTAT
ENST00000700021.1:c.1159_1161delinsTAT	ENSP00000514757.1:p.Lys387Tyr
ENST00000700022.1:c.*543_*545delinsTAT	ENSP00000514758.1:n.*543_*545delinsTAT
ENST00000700023.1:n.2362_2364delinsTAT
ENST00000700024.1:n.2596_2598delinsTAT
ENST00000706954.1:c.1204_1206delinsTAT	ENSP00000516674.1:p.Lys402Tyr
ENST00000706955.1:c.*1239_*1241delinsTAT	ENSP00000516675.1:n.*1239_*1241delinsTAT
ENST00000686459.1:c.*790_*792delinsTAT	ENSP00000508909.1:n.*790_*792delinsTAT
ENST00000688158.1:c.*1315_*1317delinsTAT	ENSP00000509254.1:n.*1315_*1317delinsTAT
ENST00000688308.1:c.1204_1206delinsTAT	ENSP00000508752.1:p.Lys402Tyr
ENST00000688922.1:c.1125_1127delinsTAT
ENST00000693560.1:c.1723_1725delinsTAT	ENSP00000509861.1:p.Lys575Tyr
ENST00000371953.8:c.1204_1206delinsTAT MANE Select	ENSP00000361021.3:p.Lys402Tyr
ENST00000371953.7:c.1204_1206delinsTAT	ENSP00000361021.3:p.Lys402Tyr
NM_000314.5:c.1204_1206delinsTAT	NP_000305.3:p.Lys402Tyr
NM_000314.6:c.1204_1206delinsTAT	NP_000305.3:p.Lys402Tyr
NM_001304717.2:c.1723_1725delinsTAT	NP_001291646.2:p.Lys575Tyr
NM_001304718.1:c.613_615delinsTAT	NP_001291647.1:p.Lys205Tyr
XM_006717926.2:c.1159_1161delinsTAT	XP_006717989.1:p.Lys387Tyr
XM_011539982.1:c.1108_1110delinsTAT	XP_011538284.1:p.Lys370Tyr
XR_945791.1:n.1774_1776delinsTAT
NM_000314.7:c.1204_1206delinsTAT	NP_000305.3:p.Lys402Tyr
NM_001304717.5:c.1723_1725delinsTAT	NP_001291646.4:p.Lys575Tyr
NM_001304718.2:c.613_615delinsTAT	NP_001291647.1:p.Lys205Tyr
NM_000314.8:c.1204_1206delinsTAT MANE Select	NP_000305.3:p.Lys402Tyr