Canonical Allele Identifier: CA930923938

Gene: PTEN

Linked Data

• dbSNP Id: rs1860613468
• gnomAD v3: 10-87960868-TTTC-T
• gnomAD v4: 10-87960868-TTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960871_87960873del , CM000672.2:g.87960871_87960873del	GRCh38
NC_000010.10:g.89720628_89720630del , CM000672.1:g.89720628_89720630del	GRCh37
NC_000010.9:g.89710608_89710610del	NCBI36
NG_007466.2:g.102433_102435del , LRG_311:g.102433_102435del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.895-23_895-21del	ENSP00000514759.2:n.895-23_895-21del
ENST00000710265.1:c.802-23_802-21del	ENSP00000518161.1:n.802-23_802-21del
ENST00000472832.3:c.802-23_802-21del	ENSP00000483066.2:n.802-23_802-21del
ENST00000688158.2:n.1537-23_1537-21del
ENST00000688922.2:c.*632-23_*632-21del	ENSP00000508742.2:n.*632-23_*632-21del
ENST00000700021.1:c.757-23_757-21del	ENSP00000514757.1:n.757-23_757-21del
ENST00000700022.1:c.*141-23_*141-21del	ENSP00000514758.1:n.*141-23_*141-21del
ENST00000700023.1:n.1960-23_1960-21del
ENST00000700024.1:n.2194-23_2194-21del
ENST00000700025.1:n.1571-23_1571-21del
ENST00000700026.1:n.439-23_439-21del
ENST00000700029.1:c.729-23_729-21del
ENST00000706954.1:c.802-23_802-21del	ENSP00000516674.1:n.802-23_802-21del
ENST00000706955.1:c.*837-23_*837-21del	ENSP00000516675.1:n.*837-23_*837-21del
ENST00000686459.1:c.*388-23_*388-21del	ENSP00000508909.1:n.*388-23_*388-21del
ENST00000688158.1:c.*913-23_*913-21del	ENSP00000509254.1:n.*913-23_*913-21del
ENST00000688308.1:c.802-23_802-21del	ENSP00000508752.1:n.802-23_802-21del
ENST00000688922.1:c.723-23_723-21del
ENST00000693560.1:c.1321-23_1321-21del	ENSP00000509861.1:n.1321-23_1321-21del
ENST00000371953.8:c.802-23_802-21del MANE Select	ENSP00000361021.3:n.802-23_802-21del
ENST00000371953.7:c.802-23_802-21del	ENSP00000361021.3:n.802-23_802-21del
ENST00000472832.2:c.229-23_229-21del	ENSP00000483066.1:n.229-23_229-21del
NM_000314.5:c.802-23_802-21del	NP_000305.3:n.802-23_802-21del
NM_000314.6:c.802-23_802-21del	NP_000305.3:n.802-23_802-21del
NM_001304717.2:c.1321-23_1321-21del	NP_001291646.2:n.1321-23_1321-21del
NM_001304718.1:c.211-23_211-21del	NP_001291647.1:n.211-23_211-21del
XM_006717926.2:c.757-23_757-21del	XP_006717989.1:n.757-23_757-21del
XM_011539981.1:c.802-23_802-21del	XP_011538283.1:n.802-23_802-21del
XM_011539982.1:c.706-23_706-21del	XP_011538284.1:n.706-23_706-21del
XR_945791.1:n.1372-23_1372-21del
NM_000314.7:c.802-23_802-21del	NP_000305.3:n.802-23_802-21del
NM_001304717.5:c.1321-23_1321-21del	NP_001291646.4:n.1321-23_1321-21del
NM_001304718.2:c.211-23_211-21del	NP_001291647.1:n.211-23_211-21del
NM_000314.8:c.802-23_802-21del MANE Select	NP_000305.3:n.802-23_802-21del