Canonical Allele Identifier: CA470974014

Gene: PTEN

Linked Data

• COSMIC: COSM921148
• MyVariant Identifiers: chr10:g.89720784del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961027del , CM000672.2:g.87961027del	GRCh38
NC_000010.10:g.89720784del , CM000672.1:g.89720784del	GRCh37
NC_000010.9:g.89710764del	NCBI36
NG_007466.2:g.102589del , LRG_311:g.102589del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1028del	ENSP00000514759.2:p.Asp343AlafsTer5
ENST00000710265.1:c.935del	ENSP00000518161.1:p.Asp312AlafsTer5
ENST00000472832.3:c.935del	ENSP00000483066.2:p.Asp312AlafsTer5
ENST00000688158.2:n.1670del
ENST00000688922.2:c.*765del	ENSP00000508742.2:n.*765del
ENST00000700021.1:c.890del	ENSP00000514757.1:p.Asp297AlafsTer5
ENST00000700022.1:c.*274del	ENSP00000514758.1:n.*274del
ENST00000700023.1:n.2093del
ENST00000700024.1:n.2327del
ENST00000700025.1:n.1704del
ENST00000700026.1:n.572del
ENST00000706954.1:c.935del	ENSP00000516674.1:p.Asp312AlafsTer5
ENST00000706955.1:c.*970del	ENSP00000516675.1:n.*970del
ENST00000686459.1:c.*521del	ENSP00000508909.1:n.*521del
ENST00000688158.1:c.*1046del	ENSP00000509254.1:n.*1046del
ENST00000688308.1:c.935del	ENSP00000508752.1:p.Asp312AlafsTer5
ENST00000688922.1:c.856del
ENST00000693560.1:c.1454del	ENSP00000509861.1:p.Asp485AlafsTer5
ENST00000371953.8:c.935del MANE Select	ENSP00000361021.3:p.Asp312AlafsTer5
ENST00000371953.7:c.935del	ENSP00000361021.3:p.Asp312AlafsTer5
ENST00000472832.2:c.362del	ENSP00000483066.1:p.Asp121AlafsTer5
NM_000314.5:c.935del	NP_000305.3:p.Asp312AlafsTer5
NM_000314.6:c.935del	NP_000305.3:p.Asp312AlafsTer5
NM_001304717.2:c.1454del	NP_001291646.2:p.Asp485AlafsTer5
NM_001304718.1:c.344del	NP_001291647.1:p.Asp115AlafsTer5
XM_006717926.2:c.890del	XP_006717989.1:p.Asp297AlafsTer5
XM_011539981.1:c.935del	XP_011538283.1:p.Asp312AlafsTer5
XM_011539982.1:c.839del	XP_011538284.1:p.Asp280AlafsTer5
XR_945791.1:n.1505del
NM_000314.7:c.935del	NP_000305.3:p.Asp312AlafsTer5
NM_001304717.5:c.1454del	NP_001291646.4:p.Asp485AlafsTer5
NM_001304718.2:c.344del	NP_001291647.1:p.Asp115AlafsTer5
NM_000314.8:c.935del MANE Select	NP_000305.3:p.Asp312AlafsTer5