Canonical Allele Identifier: CA470667614

Gene: PTEN

Linked Data

• COSMIC: COSM28898
• MyVariant Identifiers: chr10:g.89711914del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87952157del , CM000672.2:g.87952157del	GRCh38
NC_000010.10:g.89711914del , CM000672.1:g.89711914del	GRCh37
NC_000010.9:g.89701894del	NCBI36
NG_007466.2:g.93719del , LRG_311:g.93719del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.532del	ENSP00000514759.2:p.Tyr178IlefsTer5
ENST00000710265.1:c.532del	ENSP00000518161.1:p.Tyr178IlefsTer5
ENST00000472832.3:c.532del	ENSP00000483066.2:p.Tyr178IlefsTer5
ENST00000688158.2:n.1267del
ENST00000688922.2:c.*362del	ENSP00000508742.2:n.*362del
ENST00000700021.1:c.487del	ENSP00000514757.1:p.Tyr163IlefsTer5
ENST00000700022.1:c.493-5696del	ENSP00000514758.1:n.493-5696del
ENST00000700023.1:n.1690del
ENST00000700024.1:n.1924del
ENST00000700025.1:n.1301del
ENST00000700029.1:c.366del
ENST00000706954.1:c.532del	ENSP00000516674.1:p.Tyr178IlefsTer5
ENST00000706955.1:c.*567del	ENSP00000516675.1:n.*567del
ENST00000686459.1:c.*118del	ENSP00000508909.1:n.*118del
ENST00000688158.1:c.*643del	ENSP00000509254.1:n.*643del
ENST00000688308.1:c.532del	ENSP00000508752.1:p.Tyr178IlefsTer5
ENST00000688922.1:c.453del
ENST00000693560.1:c.1051del	ENSP00000509861.1:p.Tyr351IlefsTer5
ENST00000371953.8:c.532del MANE Select	ENSP00000361021.3:p.Tyr178IlefsTer5
ENST00000371953.7:c.532del	ENSP00000361021.3:p.Tyr178IlefsTer5
NM_000314.5:c.532del	NP_000305.3:p.Tyr178IlefsTer5
NM_000314.6:c.532del	NP_000305.3:p.Tyr178IlefsTer5
NM_001304717.2:c.1051del	NP_001291646.2:p.Tyr351IlefsTer5
NM_001304718.1:c.-60del	NP_001291647.1:n.-60del
XM_006717926.2:c.487del	XP_006717989.1:p.Tyr163IlefsTer5
XM_011539981.1:c.532del	XP_011538283.1:p.Tyr178IlefsTer5
XM_011539982.1:c.436del	XP_011538284.1:p.Tyr146IlefsTer5
XR_945789.1:n.1403del
XR_945790.1:n.1520del
XR_945791.1:n.1205-5696del
NM_000314.7:c.532del	NP_000305.3:p.Tyr178IlefsTer5
NM_001304717.5:c.1051del	NP_001291646.4:p.Tyr351IlefsTer5
NM_001304718.2:c.-60del	NP_001291647.1:n.-60del
NM_000314.8:c.532del MANE Select	NP_000305.3:p.Tyr178IlefsTer5