Canonical Allele Identifier: CA891838214

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965453_87965454delinsTG , CM000672.2:g.87965453_87965454delinsTG	GRCh38
NC_000010.10:g.89725210_89725211delinsTG , CM000672.1:g.89725210_89725211delinsTG	GRCh37
NC_000010.9:g.89715190_89715191delinsTG	NCBI36
NG_007466.2:g.107015_107016delinsTG , LRG_311:g.107015_107016delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1286_1287delinsTG	ENSP00000514759.2:p.Thr429Met
ENST00000710265.1:c.*222_*223delinsTG	ENSP00000518161.1:n.*222_*223delinsTG
ENST00000688158.2:n.1928_1929delinsTG
ENST00000688922.2:c.*1023_*1024delinsTG	ENSP00000508742.2:n.*1023_*1024delinsTG
ENST00000700021.1:c.1148_1149delinsTG	ENSP00000514757.1:p.Thr383Met
ENST00000700022.1:c.*532_*533delinsTG	ENSP00000514758.1:n.*532_*533delinsTG
ENST00000700023.1:n.2351_2352delinsTG
ENST00000700024.1:n.2585_2586delinsTG
ENST00000706954.1:c.1193_1194delinsTG	ENSP00000516674.1:p.Thr398Met
ENST00000706955.1:c.*1228_*1229delinsTG	ENSP00000516675.1:n.*1228_*1229delinsTG
ENST00000686459.1:c.*779_*780delinsTG	ENSP00000508909.1:n.*779_*780delinsTG
ENST00000688158.1:c.*1304_*1305delinsTG	ENSP00000509254.1:n.*1304_*1305delinsTG
ENST00000688308.1:c.1193_1194delinsTG	ENSP00000508752.1:p.Thr398Met
ENST00000688922.1:c.1114_1115delinsTG
ENST00000693560.1:c.1712_1713delinsTG	ENSP00000509861.1:p.Thr571Met
ENST00000371953.8:c.1193_1194delinsTG MANE Select	ENSP00000361021.3:p.Thr398Met
ENST00000371953.7:c.1193_1194delinsTG	ENSP00000361021.3:p.Thr398Met
NM_000314.5:c.1193_1194delinsTG	NP_000305.3:p.Thr398Met
NM_000314.6:c.1193_1194delinsTG	NP_000305.3:p.Thr398Met
NM_001304717.2:c.1712_1713delinsTG	NP_001291646.2:p.Thr571Met
NM_001304718.1:c.602_603delinsTG	NP_001291647.1:p.Thr201Met
XM_006717926.2:c.1148_1149delinsTG	XP_006717989.1:p.Thr383Met
XM_011539982.1:c.1097_1098delinsTG	XP_011538284.1:p.Thr366Met
XR_945791.1:n.1763_1764delinsTG
NM_000314.7:c.1193_1194delinsTG	NP_000305.3:p.Thr398Met
NM_001304717.5:c.1712_1713delinsTG	NP_001291646.4:p.Thr571Met
NM_001304718.2:c.602_603delinsTG	NP_001291647.1:p.Thr201Met
NM_000314.8:c.1193_1194delinsTG MANE Select	NP_000305.3:p.Thr398Met