Canonical Allele Identifier: CA645554116

Gene: PTEN

Linked Data

• COSMIC: COSM4982

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961047_87961049del , CM000672.2:g.87961047_87961049del	GRCh38
NC_000010.10:g.89720804_89720806del , CM000672.1:g.89720804_89720806del	GRCh37
NC_000010.9:g.89710784_89710786del	NCBI36
NG_007466.2:g.102609_102611del , LRG_311:g.102609_102611del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1048_1050del	ENSP00000514759.2:p.Thr350del
ENST00000710265.1:c.955_957del	ENSP00000518161.1:p.Thr319del
ENST00000472832.3:c.955_957del	ENSP00000483066.2:p.Thr319del
ENST00000688158.2:n.1690_1692del
ENST00000688922.2:c.*785_*787del	ENSP00000508742.2:n.*785_*787del
ENST00000700021.1:c.910_912del	ENSP00000514757.1:p.Thr304del
ENST00000700022.1:c.*294_*296del	ENSP00000514758.1:n.*294_*296del
ENST00000700023.1:n.2113_2115del
ENST00000700024.1:n.2347_2349del
ENST00000700025.1:n.1724_1726del
ENST00000700026.1:n.592_594del
ENST00000706954.1:c.955_957del	ENSP00000516674.1:p.Thr319del
ENST00000706955.1:c.*990_*992del	ENSP00000516675.1:n.*990_*992del
ENST00000686459.1:c.*541_*543del	ENSP00000508909.1:n.*541_*543del
ENST00000688158.1:c.*1066_*1068del	ENSP00000509254.1:n.*1066_*1068del
ENST00000688308.1:c.955_957del	ENSP00000508752.1:p.Thr319del
ENST00000688922.1:c.876_878del
ENST00000693560.1:c.1474_1476del	ENSP00000509861.1:p.Thr492del
ENST00000371953.8:c.955_957del MANE Select	ENSP00000361021.3:p.Thr319del
ENST00000371953.7:c.955_957del	ENSP00000361021.3:p.Thr319del
ENST00000472832.2:c.382_384del	ENSP00000483066.1:p.Thr128del
NM_000314.5:c.955_957del	NP_000305.3:p.Thr319del
NM_000314.6:c.955_957del	NP_000305.3:p.Thr319del
NM_001304717.2:c.1474_1476del	NP_001291646.2:p.Thr492del
NM_001304718.1:c.364_366del	NP_001291647.1:p.Thr122del
XM_006717926.2:c.910_912del	XP_006717989.1:p.Thr304del
XM_011539981.1:c.955_957del	XP_011538283.1:p.Thr319del
XM_011539982.1:c.859_861del	XP_011538284.1:p.Thr287del
XR_945791.1:n.1525_1527del
NM_000314.7:c.955_957del	NP_000305.3:p.Thr319del
NM_001304717.5:c.1474_1476del	NP_001291646.4:p.Thr492del
NM_001304718.2:c.364_366del	NP_001291647.1:p.Thr122del
NM_000314.8:c.955_957del MANE Select	NP_000305.3:p.Thr319del