Canonical Allele Identifier: CA891837488

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965357_87965358delinsTT , CM000672.2:g.87965357_87965358delinsTT	GRCh38
NC_000010.10:g.89725114_89725115delinsTT , CM000672.1:g.89725114_89725115delinsTT	GRCh37
NC_000010.9:g.89715094_89715095delinsTT	NCBI36
NG_007466.2:g.106919_106920delinsTT , LRG_311:g.106919_106920delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1190_1191delinsTT	ENSP00000514759.2:p.Thr397Ile
ENST00000710265.1:c.*126_*127delinsTT	ENSP00000518161.1:n.*126_*127delinsTT
ENST00000688158.2:n.1832_1833delinsTT
ENST00000688922.2:c.*927_*928delinsTT	ENSP00000508742.2:n.*927_*928delinsTT
ENST00000700021.1:c.1052_1053delinsTT	ENSP00000514757.1:p.Thr351Ile
ENST00000700022.1:c.*436_*437delinsTT	ENSP00000514758.1:n.*436_*437delinsTT
ENST00000700023.1:n.2255_2256delinsTT
ENST00000700024.1:n.2489_2490delinsTT
ENST00000706954.1:c.1097_1098delinsTT	ENSP00000516674.1:p.Thr366Ile
ENST00000706955.1:c.*1132_*1133delinsTT	ENSP00000516675.1:n.*1132_*1133delinsTT
ENST00000686459.1:c.*683_*684delinsTT	ENSP00000508909.1:n.*683_*684delinsTT
ENST00000688158.1:c.*1208_*1209delinsTT	ENSP00000509254.1:n.*1208_*1209delinsTT
ENST00000688308.1:c.1097_1098delinsTT	ENSP00000508752.1:p.Thr366Ile
ENST00000688922.1:c.1018_1019delinsTT
ENST00000693560.1:c.1616_1617delinsTT	ENSP00000509861.1:p.Thr539Ile
ENST00000371953.8:c.1097_1098delinsTT MANE Select	ENSP00000361021.3:p.Thr366Ile
ENST00000371953.7:c.1097_1098delinsTT	ENSP00000361021.3:p.Thr366Ile
NM_000314.5:c.1097_1098delinsTT	NP_000305.3:p.Thr366Ile
NM_000314.6:c.1097_1098delinsTT	NP_000305.3:p.Thr366Ile
NM_001304717.2:c.1616_1617delinsTT	NP_001291646.2:p.Thr539Ile
NM_001304718.1:c.506_507delinsTT	NP_001291647.1:p.Thr169Ile
XM_006717926.2:c.1052_1053delinsTT	XP_006717989.1:p.Thr351Ile
XM_011539982.1:c.1001_1002delinsTT	XP_011538284.1:p.Thr334Ile
XR_945791.1:n.1667_1668delinsTT
NM_000314.7:c.1097_1098delinsTT	NP_000305.3:p.Thr366Ile
NM_001304717.5:c.1616_1617delinsTT	NP_001291646.4:p.Thr539Ile
NM_001304718.2:c.506_507delinsTT	NP_001291647.1:p.Thr169Ile
NM_000314.8:c.1097_1098delinsTT MANE Select	NP_000305.3:p.Thr366Ile