Canonical Allele Identifier: CA470671328

Gene: PTEN

Linked Data

• COSMIC: COSM5826
• MyVariant Identifiers: chr10:g.89725138del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965381del , CM000672.2:g.87965381del	GRCh38
NC_000010.10:g.89725138del , CM000672.1:g.89725138del	GRCh37
NC_000010.9:g.89715118del	NCBI36
NG_007466.2:g.106943del , LRG_311:g.106943del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1214del	ENSP00000514759.2:p.Pro405LeufsTer?
ENST00000710265.1:c.*150del	ENSP00000518161.1:n.*150del
ENST00000688158.2:n.1856del
ENST00000688922.2:c.*951del	ENSP00000508742.2:n.*951del
ENST00000700021.1:c.1076del	ENSP00000514757.1:p.Pro359LeufsTer?
ENST00000700022.1:c.*460del	ENSP00000514758.1:n.*460del
ENST00000700023.1:n.2279del
ENST00000700024.1:n.2513del
ENST00000706954.1:c.1121del	ENSP00000516674.1:p.Pro374LeufsTer?
ENST00000706955.1:c.*1156del	ENSP00000516675.1:n.*1156del
ENST00000686459.1:c.*707del	ENSP00000508909.1:n.*707del
ENST00000688158.1:c.*1232del	ENSP00000509254.1:n.*1232del
ENST00000688308.1:c.1121del	ENSP00000508752.1:p.Pro374LeufsTer?
ENST00000688922.1:c.1042del
ENST00000693560.1:c.1640del	ENSP00000509861.1:p.Pro547LeufsTer?
ENST00000371953.8:c.1121del MANE Select	ENSP00000361021.3:p.Pro374LeufsTer?
ENST00000371953.7:c.1121del	ENSP00000361021.3:p.Pro374LeufsTer?
NM_000314.5:c.1121del	NP_000305.3:p.Pro374LeufsTer?
NM_000314.6:c.1121del	NP_000305.3:p.Pro374LeufsTer?
NM_001304717.2:c.1640del	NP_001291646.2:p.Pro547LeufsTer?
NM_001304718.1:c.530del	NP_001291647.1:p.Pro177LeufsTer?
XM_006717926.2:c.1076del	XP_006717989.1:p.Pro359LeufsTer?
XM_011539982.1:c.1025del	XP_011538284.1:p.Pro342LeufsTer?
XR_945791.1:n.1691del
NM_000314.7:c.1121del	NP_000305.3:p.Pro374LeufsTer?
NM_001304717.5:c.1640del	NP_001291646.4:p.Pro547LeufsTer?
NM_001304718.2:c.530del	NP_001291647.1:p.Pro177LeufsTer?
NM_000314.8:c.1121del MANE Select	NP_000305.3:p.Pro374LeufsTer?