Canonical Allele Identifier: CA594923685

Gene: PTEN

Linked Data

• dbSNP Id: rs1564568115
• gnomAD v2: 10-89720604-AAAT-A
• gnomAD v4: 10-87960847-AAAT-A
• MyVariant Identifiers: chr10:g.89720605_89720607del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960849_87960851del , CM000672.2:g.87960849_87960851del	GRCh38
NC_000010.10:g.89720606_89720608del , CM000672.1:g.89720606_89720608del	GRCh37
NC_000010.9:g.89710586_89710588del	NCBI36
NG_007466.2:g.102411_102413del , LRG_311:g.102411_102413del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-45_895-43del	ENSP00000514759.2:n.895-45_895-43del
ENST00000710265.1:c.802-45_802-43del	ENSP00000518161.1:n.802-45_802-43del
ENST00000472832.3:c.802-45_802-43del	ENSP00000483066.2:n.802-45_802-43del
ENST00000688158.2:n.1537-45_1537-43del
ENST00000688922.2:c.*632-45_*632-43del	ENSP00000508742.2:n.*632-45_*632-43del
ENST00000700021.1:c.757-45_757-43del	ENSP00000514757.1:n.757-45_757-43del
ENST00000700022.1:c.*141-45_*141-43del	ENSP00000514758.1:n.*141-45_*141-43del
ENST00000700023.1:n.1960-45_1960-43del
ENST00000700024.1:n.2194-45_2194-43del
ENST00000700025.1:n.1571-45_1571-43del
ENST00000700026.1:n.439-45_439-43del
ENST00000700029.1:c.729-45_729-43del
ENST00000706954.1:c.802-45_802-43del	ENSP00000516674.1:n.802-45_802-43del
ENST00000706955.1:c.*837-45_*837-43del	ENSP00000516675.1:n.*837-45_*837-43del
ENST00000686459.1:c.*388-45_*388-43del	ENSP00000508909.1:n.*388-45_*388-43del
ENST00000688158.1:c.*913-45_*913-43del	ENSP00000509254.1:n.*913-45_*913-43del
ENST00000688308.1:c.802-45_802-43del	ENSP00000508752.1:n.802-45_802-43del
ENST00000688922.1:c.723-45_723-43del
ENST00000693560.1:c.1321-45_1321-43del	ENSP00000509861.1:n.1321-45_1321-43del
ENST00000371953.8:c.802-45_802-43del MANE Select	ENSP00000361021.3:n.802-45_802-43del
ENST00000371953.7:c.802-45_802-43del	ENSP00000361021.3:n.802-45_802-43del
ENST00000472832.2:c.229-45_229-43del	ENSP00000483066.1:n.229-45_229-43del
NM_000314.5:c.802-45_802-43del	NP_000305.3:n.802-45_802-43del
NM_000314.6:c.802-45_802-43del	NP_000305.3:n.802-45_802-43del
NM_001304717.2:c.1321-45_1321-43del	NP_001291646.2:n.1321-45_1321-43del
NM_001304718.1:c.211-45_211-43del	NP_001291647.1:n.211-45_211-43del
XM_006717926.2:c.757-45_757-43del	XP_006717989.1:n.757-45_757-43del
XM_011539981.1:c.802-45_802-43del	XP_011538283.1:n.802-45_802-43del
XM_011539982.1:c.706-45_706-43del	XP_011538284.1:n.706-45_706-43del
XR_945791.1:n.1372-45_1372-43del
NM_000314.7:c.802-45_802-43del	NP_000305.3:n.802-45_802-43del
NM_001304717.5:c.1321-45_1321-43del	NP_001291646.4:n.1321-45_1321-43del
NM_001304718.2:c.211-45_211-43del	NP_001291647.1:n.211-45_211-43del
NM_000314.8:c.802-45_802-43del MANE Select	NP_000305.3:n.802-45_802-43del