Canonical Allele Identifier: CA2501039502

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960820_87960834del , CM000672.2:g.87960820_87960834del	GRCh38
NC_000010.10:g.89720577_89720591del , CM000672.1:g.89720577_89720591del	GRCh37
NC_000010.9:g.89710557_89710571del	NCBI36
NG_007466.2:g.102382_102396del , LRG_311:g.102382_102396del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.895-74_895-60del	ENSP00000514759.2:n.895-74_895-60del
ENST00000710265.1:c.802-74_802-60del	ENSP00000518161.1:n.802-74_802-60del
ENST00000472832.3:c.802-74_802-60del	ENSP00000483066.2:n.802-74_802-60del
ENST00000688158.2:n.1537-74_1537-60del
ENST00000688922.2:c.*632-74_*632-60del	ENSP00000508742.2:n.*632-74_*632-60del
ENST00000700021.1:c.757-74_757-60del	ENSP00000514757.1:n.757-74_757-60del
ENST00000700022.1:c.*141-74_*141-60del	ENSP00000514758.1:n.*141-74_*141-60del
ENST00000700023.1:n.1960-74_1960-60del
ENST00000700024.1:n.2194-74_2194-60del
ENST00000700025.1:n.1571-74_1571-60del
ENST00000700026.1:n.439-74_439-60del
ENST00000700029.1:c.729-74_729-60del
ENST00000706954.1:c.802-74_802-60del	ENSP00000516674.1:n.802-74_802-60del
ENST00000706955.1:c.*837-74_*837-60del	ENSP00000516675.1:n.*837-74_*837-60del
ENST00000686459.1:c.*388-74_*388-60del	ENSP00000508909.1:n.*388-74_*388-60del
ENST00000688158.1:c.*913-74_*913-60del	ENSP00000509254.1:n.*913-74_*913-60del
ENST00000688308.1:c.802-74_802-60del	ENSP00000508752.1:n.802-74_802-60del
ENST00000688922.1:c.723-74_723-60del
ENST00000693560.1:c.1321-74_1321-60del	ENSP00000509861.1:n.1321-74_1321-60del
ENST00000371953.8:c.802-74_802-60del MANE Select	ENSP00000361021.3:n.802-74_802-60del
ENST00000371953.7:c.802-74_802-60del	ENSP00000361021.3:n.802-74_802-60del
ENST00000472832.2:c.229-74_229-60del	ENSP00000483066.1:n.229-74_229-60del
NM_000314.5:c.802-74_802-60del	NP_000305.3:n.802-74_802-60del
NM_000314.6:c.802-74_802-60del	NP_000305.3:n.802-74_802-60del
NM_001304717.2:c.1321-74_1321-60del	NP_001291646.2:n.1321-74_1321-60del
NM_001304718.1:c.211-74_211-60del	NP_001291647.1:n.211-74_211-60del
XM_006717926.2:c.757-74_757-60del	XP_006717989.1:n.757-74_757-60del
XM_011539981.1:c.802-74_802-60del	XP_011538283.1:n.802-74_802-60del
XM_011539982.1:c.706-74_706-60del	XP_011538284.1:n.706-74_706-60del
XR_945791.1:n.1372-74_1372-60del
NM_000314.7:c.802-74_802-60del	NP_000305.3:n.802-74_802-60del
NM_001304717.5:c.1321-74_1321-60del	NP_001291646.4:n.1321-74_1321-60del
NM_001304718.2:c.211-74_211-60del	NP_001291647.1:n.211-74_211-60del
NM_000314.8:c.802-74_802-60del MANE Select	NP_000305.3:n.802-74_802-60del