Canonical Allele Identifier: CA891841727

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965461_87965463delinsGAT , CM000672.2:g.87965461_87965463delinsGAT	GRCh38
NC_000010.10:g.89725218_89725220delinsGAT , CM000672.1:g.89725218_89725220delinsGAT	GRCh37
NC_000010.9:g.89715198_89715200delinsGAT	NCBI36
NG_007466.2:g.107023_107025delinsGAT , LRG_311:g.107023_107025delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1294_1296delinsGAT	ENSP00000514759.2:p.Thr432Asp
ENST00000710265.1:c.*230_*232delinsGAT	ENSP00000518161.1:n.*230_*232delinsGAT
ENST00000688158.2:n.1936_1938delinsGAT
ENST00000688922.2:c.*1031_*1033delinsGAT	ENSP00000508742.2:n.*1031_*1033delinsGAT
ENST00000700021.1:c.1156_1158delinsGAT	ENSP00000514757.1:p.Thr386Asp
ENST00000700022.1:c.*540_*542delinsGAT	ENSP00000514758.1:n.*540_*542delinsGAT
ENST00000700023.1:n.2359_2361delinsGAT
ENST00000700024.1:n.2593_2595delinsGAT
ENST00000706954.1:c.1201_1203delinsGAT	ENSP00000516674.1:p.Thr401Asp
ENST00000706955.1:c.*1236_*1238delinsGAT	ENSP00000516675.1:n.*1236_*1238delinsGAT
ENST00000686459.1:c.*787_*789delinsGAT	ENSP00000508909.1:n.*787_*789delinsGAT
ENST00000688158.1:c.*1312_*1314delinsGAT	ENSP00000509254.1:n.*1312_*1314delinsGAT
ENST00000688308.1:c.1201_1203delinsGAT	ENSP00000508752.1:p.Thr401Asp
ENST00000688922.1:c.1122_1124delinsGAT
ENST00000693560.1:c.1720_1722delinsGAT	ENSP00000509861.1:p.Thr574Asp
ENST00000371953.8:c.1201_1203delinsGAT MANE Select	ENSP00000361021.3:p.Thr401Asp
ENST00000371953.7:c.1201_1203delinsGAT	ENSP00000361021.3:p.Thr401Asp
NM_000314.5:c.1201_1203delinsGAT	NP_000305.3:p.Thr401Asp
NM_000314.6:c.1201_1203delinsGAT	NP_000305.3:p.Thr401Asp
NM_001304717.2:c.1720_1722delinsGAT	NP_001291646.2:p.Thr574Asp
NM_001304718.1:c.610_612delinsGAT	NP_001291647.1:p.Thr204Asp
XM_006717926.2:c.1156_1158delinsGAT	XP_006717989.1:p.Thr386Asp
XM_011539982.1:c.1105_1107delinsGAT	XP_011538284.1:p.Thr369Asp
XR_945791.1:n.1771_1773delinsGAT
NM_000314.7:c.1201_1203delinsGAT	NP_000305.3:p.Thr401Asp
NM_001304717.5:c.1720_1722delinsGAT	NP_001291646.4:p.Thr574Asp
NM_001304718.2:c.610_612delinsGAT	NP_001291647.1:p.Thr204Asp
NM_000314.8:c.1201_1203delinsGAT MANE Select	NP_000305.3:p.Thr401Asp