Canonical Allele Identifier: CA1926189817

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960721_87960722delinsCT , CM000672.2:g.87960721_87960722delinsCT	GRCh38
NC_000010.10:g.89720478_89720479delinsCT , CM000672.1:g.89720478_89720479delinsCT	GRCh37
NC_000010.9:g.89710458_89710459delinsCT	NCBI36
NG_007466.2:g.102283_102284delinsCT , LRG_311:g.102283_102284delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.895-173_895-172delinsCT	ENSP00000514759.2:n.895-173_895-172delinsCT
ENST00000710265.1:c.802-173_802-172delinsCT	ENSP00000518161.1:n.802-173_802-172delinsCT
ENST00000472832.3:c.802-173_802-172delinsCT	ENSP00000483066.2:n.802-173_802-172delinsCT
ENST00000688158.2:n.1537-173_1537-172delinsCT
ENST00000688922.2:c.*632-173_*632-172delinsCT	ENSP00000508742.2:n.*632-173_*632-172delinsCT
ENST00000700021.1:c.757-173_757-172delinsCT	ENSP00000514757.1:n.757-173_757-172delinsCT
ENST00000700022.1:c.*141-173_*141-172delinsCT	ENSP00000514758.1:n.*141-173_*141-172delinsCT
ENST00000700023.1:n.1960-173_1960-172delinsCT
ENST00000700024.1:n.2194-173_2194-172delinsCT
ENST00000700025.1:n.1571-173_1571-172delinsCT
ENST00000700026.1:n.439-173_439-172delinsCT
ENST00000700029.1:c.729-173_729-172delinsCT
ENST00000706954.1:c.802-173_802-172delinsCT	ENSP00000516674.1:n.802-173_802-172delinsCT
ENST00000706955.1:c.*837-173_*837-172delinsCT	ENSP00000516675.1:n.*837-173_*837-172delinsCT
ENST00000686459.1:c.*388-173_*388-172delinsCT	ENSP00000508909.1:n.*388-173_*388-172delinsCT
ENST00000688158.1:c.*913-173_*913-172delinsCT	ENSP00000509254.1:n.*913-173_*913-172delinsCT
ENST00000688308.1:c.802-173_802-172delinsCT	ENSP00000508752.1:n.802-173_802-172delinsCT
ENST00000688922.1:c.723-173_723-172delinsCT
ENST00000693560.1:c.1321-173_1321-172delinsCT	ENSP00000509861.1:n.1321-173_1321-172delinsCT
ENST00000371953.8:c.802-173_802-172delinsCT MANE Select	ENSP00000361021.3:n.802-173_802-172delinsCT
ENST00000371953.7:c.802-173_802-172delinsCT	ENSP00000361021.3:n.802-173_802-172delinsCT
ENST00000472832.2:c.229-173_229-172delinsCT	ENSP00000483066.1:n.229-173_229-172delinsCT
NM_000314.5:c.802-173_802-172delinsCT	NP_000305.3:n.802-173_802-172delinsCT
NM_000314.6:c.802-173_802-172delinsCT	NP_000305.3:n.802-173_802-172delinsCT
NM_001304717.2:c.1321-173_1321-172delinsCT	NP_001291646.2:n.1321-173_1321-172delinsCT
NM_001304718.1:c.211-173_211-172delinsCT	NP_001291647.1:n.211-173_211-172delinsCT
XM_006717926.2:c.757-173_757-172delinsCT	XP_006717989.1:n.757-173_757-172delinsCT
XM_011539981.1:c.802-173_802-172delinsCT	XP_011538283.1:n.802-173_802-172delinsCT
XM_011539982.1:c.706-173_706-172delinsCT	XP_011538284.1:n.706-173_706-172delinsCT
XR_945791.1:n.1372-173_1372-172delinsCT
NM_000314.7:c.802-173_802-172delinsCT	NP_000305.3:n.802-173_802-172delinsCT
NM_001304717.5:c.1321-173_1321-172delinsCT	NP_001291646.4:n.1321-173_1321-172delinsCT
NM_001304718.2:c.211-173_211-172delinsCT	NP_001291647.1:n.211-173_211-172delinsCT
NM_000314.8:c.802-173_802-172delinsCT MANE Select	NP_000305.3:n.802-173_802-172delinsCT