Canonical Allele Identifier: CA1926189829

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960744_87960745delinsCT , CM000672.2:g.87960744_87960745delinsCT	GRCh38
NC_000010.10:g.89720501_89720502delinsCT , CM000672.1:g.89720501_89720502delinsCT	GRCh37
NC_000010.9:g.89710481_89710482delinsCT	NCBI36
NG_007466.2:g.102306_102307delinsCT , LRG_311:g.102306_102307delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-150_895-149delinsCT	ENSP00000514759.2:n.895-150_895-149delinsCT
ENST00000710265.1:c.802-150_802-149delinsCT	ENSP00000518161.1:n.802-150_802-149delinsCT
ENST00000472832.3:c.802-150_802-149delinsCT	ENSP00000483066.2:n.802-150_802-149delinsCT
ENST00000688158.2:n.1537-150_1537-149delinsCT
ENST00000688922.2:c.*632-150_*632-149delinsCT	ENSP00000508742.2:n.*632-150_*632-149delinsCT
ENST00000700021.1:c.757-150_757-149delinsCT	ENSP00000514757.1:n.757-150_757-149delinsCT
ENST00000700022.1:c.*141-150_*141-149delinsCT	ENSP00000514758.1:n.*141-150_*141-149delinsCT
ENST00000700023.1:n.1960-150_1960-149delinsCT
ENST00000700024.1:n.2194-150_2194-149delinsCT
ENST00000700025.1:n.1571-150_1571-149delinsCT
ENST00000700026.1:n.439-150_439-149delinsCT
ENST00000700029.1:c.729-150_729-149delinsCT
ENST00000706954.1:c.802-150_802-149delinsCT	ENSP00000516674.1:n.802-150_802-149delinsCT
ENST00000706955.1:c.*837-150_*837-149delinsCT	ENSP00000516675.1:n.*837-150_*837-149delinsCT
ENST00000686459.1:c.*388-150_*388-149delinsCT	ENSP00000508909.1:n.*388-150_*388-149delinsCT
ENST00000688158.1:c.*913-150_*913-149delinsCT	ENSP00000509254.1:n.*913-150_*913-149delinsCT
ENST00000688308.1:c.802-150_802-149delinsCT	ENSP00000508752.1:n.802-150_802-149delinsCT
ENST00000688922.1:c.723-150_723-149delinsCT
ENST00000693560.1:c.1321-150_1321-149delinsCT	ENSP00000509861.1:n.1321-150_1321-149delinsCT
ENST00000371953.8:c.802-150_802-149delinsCT MANE Select	ENSP00000361021.3:n.802-150_802-149delinsCT
ENST00000371953.7:c.802-150_802-149delinsCT	ENSP00000361021.3:n.802-150_802-149delinsCT
ENST00000472832.2:c.229-150_229-149delinsCT	ENSP00000483066.1:n.229-150_229-149delinsCT
NM_000314.5:c.802-150_802-149delinsCT	NP_000305.3:n.802-150_802-149delinsCT
NM_000314.6:c.802-150_802-149delinsCT	NP_000305.3:n.802-150_802-149delinsCT
NM_001304717.2:c.1321-150_1321-149delinsCT	NP_001291646.2:n.1321-150_1321-149delinsCT
NM_001304718.1:c.211-150_211-149delinsCT	NP_001291647.1:n.211-150_211-149delinsCT
XM_006717926.2:c.757-150_757-149delinsCT	XP_006717989.1:n.757-150_757-149delinsCT
XM_011539981.1:c.802-150_802-149delinsCT	XP_011538283.1:n.802-150_802-149delinsCT
XM_011539982.1:c.706-150_706-149delinsCT	XP_011538284.1:n.706-150_706-149delinsCT
XR_945791.1:n.1372-150_1372-149delinsCT
NM_000314.7:c.802-150_802-149delinsCT	NP_000305.3:n.802-150_802-149delinsCT
NM_001304717.5:c.1321-150_1321-149delinsCT	NP_001291646.4:n.1321-150_1321-149delinsCT
NM_001304718.2:c.211-150_211-149delinsCT	NP_001291647.1:n.211-150_211-149delinsCT
NM_000314.8:c.802-150_802-149delinsCT MANE Select	NP_000305.3:n.802-150_802-149delinsCT