Canonical Allele Identifier: CA891836609

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961053_87961055delinsGAT , CM000672.2:g.87961053_87961055delinsGAT	GRCh38
NC_000010.10:g.89720810_89720812delinsGAT , CM000672.1:g.89720810_89720812delinsGAT	GRCh37
NC_000010.9:g.89710790_89710792delinsGAT	NCBI36
NG_007466.2:g.102615_102617delinsGAT , LRG_311:g.102615_102617delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1054_1056delinsGAT	ENSP00000514759.2:p.Thr352Asp
ENST00000710265.1:c.961_963delinsGAT	ENSP00000518161.1:p.Thr321Asp
ENST00000472832.3:c.961_963delinsGAT	ENSP00000483066.2:p.Thr321Asp
ENST00000688158.2:n.1696_1698delinsGAT
ENST00000688922.2:c.*791_*793delinsGAT	ENSP00000508742.2:n.*791_*793delinsGAT
ENST00000700021.1:c.916_918delinsGAT	ENSP00000514757.1:p.Thr306Asp
ENST00000700022.1:c.*300_*302delinsGAT	ENSP00000514758.1:n.*300_*302delinsGAT
ENST00000700023.1:n.2119_2121delinsGAT
ENST00000700024.1:n.2353_2355delinsGAT
ENST00000700025.1:n.1730_1732delinsGAT
ENST00000700026.1:n.598_600delinsGAT
ENST00000706954.1:c.961_963delinsGAT	ENSP00000516674.1:p.Thr321Asp
ENST00000706955.1:c.*996_*998delinsGAT	ENSP00000516675.1:n.*996_*998delinsGAT
ENST00000686459.1:c.*547_*549delinsGAT	ENSP00000508909.1:n.*547_*549delinsGAT
ENST00000688158.1:c.*1072_*1074delinsGAT	ENSP00000509254.1:n.*1072_*1074delinsGAT
ENST00000688308.1:c.961_963delinsGAT	ENSP00000508752.1:p.Thr321Asp
ENST00000688922.1:c.882_884delinsGAT
ENST00000693560.1:c.1480_1482delinsGAT	ENSP00000509861.1:p.Thr494Asp
ENST00000371953.8:c.961_963delinsGAT MANE Select	ENSP00000361021.3:p.Thr321Asp
ENST00000371953.7:c.961_963delinsGAT	ENSP00000361021.3:p.Thr321Asp
ENST00000472832.2:c.388_390delinsGAT	ENSP00000483066.1:p.Thr130Asp
NM_000314.5:c.961_963delinsGAT	NP_000305.3:p.Thr321Asp
NM_000314.6:c.961_963delinsGAT	NP_000305.3:p.Thr321Asp
NM_001304717.2:c.1480_1482delinsGAT	NP_001291646.2:p.Thr494Asp
NM_001304718.1:c.370_372delinsGAT	NP_001291647.1:p.Thr124Asp
XM_006717926.2:c.916_918delinsGAT	XP_006717989.1:p.Thr306Asp
XM_011539981.1:c.961_963delinsGAT	XP_011538283.1:p.Thr321Asp
XM_011539982.1:c.865_867delinsGAT	XP_011538284.1:p.Thr289Asp
XR_945791.1:n.1531_1533delinsGAT
NM_000314.7:c.961_963delinsGAT	NP_000305.3:p.Thr321Asp
NM_001304717.5:c.1480_1482delinsGAT	NP_001291646.4:p.Thr494Asp
NM_001304718.2:c.370_372delinsGAT	NP_001291647.1:p.Thr124Asp
NM_000314.8:c.961_963delinsGAT MANE Select	NP_000305.3:p.Thr321Asp