Canonical Allele Identifier: CA1926189838

Gene: PTEN

Linked Data

• dbSNP Id: rs1310208607

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960785_87960787del , CM000672.2:g.87960785_87960787del	GRCh38
NC_000010.10:g.89720542_89720544del , CM000672.1:g.89720542_89720544del	GRCh37
NC_000010.9:g.89710522_89710524del	NCBI36
NG_007466.2:g.102347_102349del , LRG_311:g.102347_102349del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.895-109_895-107del	ENSP00000514759.2:n.895-109_895-107del
ENST00000710265.1:c.802-109_802-107del	ENSP00000518161.1:n.802-109_802-107del
ENST00000472832.3:c.802-109_802-107del	ENSP00000483066.2:n.802-109_802-107del
ENST00000688158.2:n.1537-109_1537-107del
ENST00000688922.2:c.*632-109_*632-107del	ENSP00000508742.2:n.*632-109_*632-107del
ENST00000700021.1:c.757-109_757-107del	ENSP00000514757.1:n.757-109_757-107del
ENST00000700022.1:c.*141-109_*141-107del	ENSP00000514758.1:n.*141-109_*141-107del
ENST00000700023.1:n.1960-109_1960-107del
ENST00000700024.1:n.2194-109_2194-107del
ENST00000700025.1:n.1571-109_1571-107del
ENST00000700026.1:n.439-109_439-107del
ENST00000700029.1:c.729-109_729-107del
ENST00000706954.1:c.802-109_802-107del	ENSP00000516674.1:n.802-109_802-107del
ENST00000706955.1:c.*837-109_*837-107del	ENSP00000516675.1:n.*837-109_*837-107del
ENST00000686459.1:c.*388-109_*388-107del	ENSP00000508909.1:n.*388-109_*388-107del
ENST00000688158.1:c.*913-109_*913-107del	ENSP00000509254.1:n.*913-109_*913-107del
ENST00000688308.1:c.802-109_802-107del	ENSP00000508752.1:n.802-109_802-107del
ENST00000688922.1:c.723-109_723-107del
ENST00000693560.1:c.1321-109_1321-107del	ENSP00000509861.1:n.1321-109_1321-107del
ENST00000371953.8:c.802-109_802-107del MANE Select	ENSP00000361021.3:n.802-109_802-107del
ENST00000371953.7:c.802-109_802-107del	ENSP00000361021.3:n.802-109_802-107del
ENST00000472832.2:c.229-109_229-107del	ENSP00000483066.1:n.229-109_229-107del
NM_000314.5:c.802-109_802-107del	NP_000305.3:n.802-109_802-107del
NM_000314.6:c.802-109_802-107del	NP_000305.3:n.802-109_802-107del
NM_001304717.2:c.1321-109_1321-107del	NP_001291646.2:n.1321-109_1321-107del
NM_001304718.1:c.211-109_211-107del	NP_001291647.1:n.211-109_211-107del
XM_006717926.2:c.757-109_757-107del	XP_006717989.1:n.757-109_757-107del
XM_011539981.1:c.802-109_802-107del	XP_011538283.1:n.802-109_802-107del
XM_011539982.1:c.706-109_706-107del	XP_011538284.1:n.706-109_706-107del
XR_945791.1:n.1372-109_1372-107del
NM_000314.7:c.802-109_802-107del	NP_000305.3:n.802-109_802-107del
NM_001304717.5:c.1321-109_1321-107del	NP_001291646.4:n.1321-109_1321-107del
NM_001304718.2:c.211-109_211-107del	NP_001291647.1:n.211-109_211-107del
NM_000314.8:c.802-109_802-107del MANE Select	NP_000305.3:n.802-109_802-107del