Canonical Allele Identifier: CA2526095200

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960710_87960714del , CM000672.2:g.87960710_87960714del	GRCh38
NC_000010.10:g.89720467_89720471del , CM000672.1:g.89720467_89720471del	GRCh37
NC_000010.9:g.89710447_89710451del	NCBI36
NG_007466.2:g.102272_102276del , LRG_311:g.102272_102276del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.895-184_895-180del	ENSP00000514759.2:n.895-184_895-180del
ENST00000710265.1:c.802-184_802-180del	ENSP00000518161.1:n.802-184_802-180del
ENST00000472832.3:c.802-184_802-180del	ENSP00000483066.2:n.802-184_802-180del
ENST00000688158.2:n.1537-184_1537-180del
ENST00000688922.2:c.*632-184_*632-180del	ENSP00000508742.2:n.*632-184_*632-180del
ENST00000700021.1:c.757-184_757-180del	ENSP00000514757.1:n.757-184_757-180del
ENST00000700022.1:c.*141-184_*141-180del	ENSP00000514758.1:n.*141-184_*141-180del
ENST00000700023.1:n.1960-184_1960-180del
ENST00000700024.1:n.2194-184_2194-180del
ENST00000700025.1:n.1571-184_1571-180del
ENST00000700026.1:n.439-184_439-180del
ENST00000700029.1:c.729-184_729-180del
ENST00000706954.1:c.802-184_802-180del	ENSP00000516674.1:n.802-184_802-180del
ENST00000706955.1:c.*837-184_*837-180del	ENSP00000516675.1:n.*837-184_*837-180del
ENST00000686459.1:c.*388-184_*388-180del	ENSP00000508909.1:n.*388-184_*388-180del
ENST00000688158.1:c.*913-184_*913-180del	ENSP00000509254.1:n.*913-184_*913-180del
ENST00000688308.1:c.802-184_802-180del	ENSP00000508752.1:n.802-184_802-180del
ENST00000688922.1:c.723-184_723-180del
ENST00000693560.1:c.1321-184_1321-180del	ENSP00000509861.1:n.1321-184_1321-180del
ENST00000371953.8:c.802-184_802-180del MANE Select	ENSP00000361021.3:n.802-184_802-180del
ENST00000371953.7:c.802-184_802-180del	ENSP00000361021.3:n.802-184_802-180del
ENST00000472832.2:c.229-184_229-180del	ENSP00000483066.1:n.229-184_229-180del
NM_000314.5:c.802-184_802-180del	NP_000305.3:n.802-184_802-180del
NM_000314.6:c.802-184_802-180del	NP_000305.3:n.802-184_802-180del
NM_001304717.2:c.1321-184_1321-180del	NP_001291646.2:n.1321-184_1321-180del
NM_001304718.1:c.211-184_211-180del	NP_001291647.1:n.211-184_211-180del
XM_006717926.2:c.757-184_757-180del	XP_006717989.1:n.757-184_757-180del
XM_011539981.1:c.802-184_802-180del	XP_011538283.1:n.802-184_802-180del
XM_011539982.1:c.706-184_706-180del	XP_011538284.1:n.706-184_706-180del
XR_945791.1:n.1372-184_1372-180del
NM_000314.7:c.802-184_802-180del	NP_000305.3:n.802-184_802-180del
NM_001304717.5:c.1321-184_1321-180del	NP_001291646.4:n.1321-184_1321-180del
NM_001304718.2:c.211-184_211-180del	NP_001291647.1:n.211-184_211-180del
NM_000314.8:c.802-184_802-180del MANE Select	NP_000305.3:n.802-184_802-180del