Canonical Allele Identifier: CA211251878

Gene: PTEN

Linked Data

• dbSNP Id: rs895004434
• gnomAD v3: 10-87960809-CAG-C
• gnomAD v4: 10-87960809-CAG-C
• MyVariant Identifiers: chr10:g.89720567_89720568del (hg19) ; chr10:g.87960810_87960811del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960811_87960812del , CM000672.2:g.87960811_87960812del	GRCh38
NC_000010.10:g.89720568_89720569del , CM000672.1:g.89720568_89720569del	GRCh37
NC_000010.9:g.89710548_89710549del	NCBI36
NG_007466.2:g.102373_102374del , LRG_311:g.102373_102374del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-83_895-82del	ENSP00000514759.2:n.895-83_895-82del
ENST00000710265.1:c.802-83_802-82del	ENSP00000518161.1:n.802-83_802-82del
ENST00000472832.3:c.802-83_802-82del	ENSP00000483066.2:n.802-83_802-82del
ENST00000688158.2:n.1537-83_1537-82del
ENST00000688922.2:c.*632-83_*632-82del	ENSP00000508742.2:n.*632-83_*632-82del
ENST00000700021.1:c.757-83_757-82del	ENSP00000514757.1:n.757-83_757-82del
ENST00000700022.1:c.*141-83_*141-82del	ENSP00000514758.1:n.*141-83_*141-82del
ENST00000700023.1:n.1960-83_1960-82del
ENST00000700024.1:n.2194-83_2194-82del
ENST00000700025.1:n.1571-83_1571-82del
ENST00000700026.1:n.439-83_439-82del
ENST00000700029.1:c.729-83_729-82del
ENST00000706954.1:c.802-83_802-82del	ENSP00000516674.1:n.802-83_802-82del
ENST00000706955.1:c.*837-83_*837-82del	ENSP00000516675.1:n.*837-83_*837-82del
ENST00000686459.1:c.*388-83_*388-82del	ENSP00000508909.1:n.*388-83_*388-82del
ENST00000688158.1:c.*913-83_*913-82del	ENSP00000509254.1:n.*913-83_*913-82del
ENST00000688308.1:c.802-83_802-82del	ENSP00000508752.1:n.802-83_802-82del
ENST00000688922.1:c.723-83_723-82del
ENST00000693560.1:c.1321-83_1321-82del	ENSP00000509861.1:n.1321-83_1321-82del
ENST00000371953.8:c.802-83_802-82del MANE Select	ENSP00000361021.3:n.802-83_802-82del
ENST00000371953.7:c.802-83_802-82del	ENSP00000361021.3:n.802-83_802-82del
ENST00000472832.2:c.229-83_229-82del	ENSP00000483066.1:n.229-83_229-82del
NM_000314.5:c.802-83_802-82del	NP_000305.3:n.802-83_802-82del
NM_000314.6:c.802-83_802-82del	NP_000305.3:n.802-83_802-82del
NM_001304717.2:c.1321-83_1321-82del	NP_001291646.2:n.1321-83_1321-82del
NM_001304718.1:c.211-83_211-82del	NP_001291647.1:n.211-83_211-82del
XM_006717926.2:c.757-83_757-82del	XP_006717989.1:n.757-83_757-82del
XM_011539981.1:c.802-83_802-82del	XP_011538283.1:n.802-83_802-82del
XM_011539982.1:c.706-83_706-82del	XP_011538284.1:n.706-83_706-82del
XR_945791.1:n.1372-83_1372-82del
NM_000314.7:c.802-83_802-82del	NP_000305.3:n.802-83_802-82del
NM_001304717.5:c.1321-83_1321-82del	NP_001291646.4:n.1321-83_1321-82del
NM_001304718.2:c.211-83_211-82del	NP_001291647.1:n.211-83_211-82del
NM_000314.8:c.802-83_802-82del MANE Select	NP_000305.3:n.802-83_802-82del