Canonical Allele Identifier: CA891839459

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957886_87957887delinsCT , CM000672.2:g.87957886_87957887delinsCT	GRCh38
NC_000010.10:g.89717643_89717644delinsCT , CM000672.1:g.89717643_89717644delinsCT	GRCh37
NC_000010.9:g.89707623_89707624delinsCT	NCBI36
NG_007466.2:g.99448_99449delinsCT , LRG_311:g.99448_99449delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.668_669delinsCT	ENSP00000514759.2:p.Lys223Thr
ENST00000710265.1:c.668_669delinsCT	ENSP00000518161.1:p.Lys223Thr
ENST00000472832.3:c.668_669delinsCT	ENSP00000483066.2:p.Lys223Thr
ENST00000688158.2:n.1403_1404delinsCT
ENST00000688922.2:c.*498_*499delinsCT	ENSP00000508742.2:n.*498_*499delinsCT
ENST00000700021.1:c.623_624delinsCT	ENSP00000514757.1:p.Lys208Thr
ENST00000700022.1:c.*7_*8delinsCT	ENSP00000514758.1:n.*7_*8delinsCT
ENST00000700023.1:n.1826_1827delinsCT
ENST00000700024.1:n.2060_2061delinsCT
ENST00000700025.1:n.1437_1438delinsCT
ENST00000700026.1:n.305_306delinsCT
ENST00000700029.1:c.502_503delinsCT
ENST00000706954.1:c.668_669delinsCT	ENSP00000516674.1:p.Lys223Thr
ENST00000706955.1:c.*703_*704delinsCT	ENSP00000516675.1:n.*703_*704delinsCT
ENST00000686459.1:c.*254_*255delinsCT	ENSP00000508909.1:n.*254_*255delinsCT
ENST00000688158.1:c.*779_*780delinsCT	ENSP00000509254.1:n.*779_*780delinsCT
ENST00000688308.1:c.668_669delinsCT	ENSP00000508752.1:p.Lys223Thr
ENST00000688922.1:c.589_590delinsCT
ENST00000693560.1:c.1187_1188delinsCT	ENSP00000509861.1:p.Lys396Thr
ENST00000371953.8:c.668_669delinsCT MANE Select	ENSP00000361021.3:p.Lys223Thr
ENST00000371953.7:c.668_669delinsCT	ENSP00000361021.3:p.Lys223Thr
ENST00000472832.2:c.95_96delinsCT	ENSP00000483066.1:p.Lys32Thr
NM_000314.5:c.668_669delinsCT	NP_000305.3:p.Lys223Thr
NM_000314.6:c.668_669delinsCT	NP_000305.3:p.Lys223Thr
NM_001304717.2:c.1187_1188delinsCT	NP_001291646.2:p.Lys396Thr
NM_001304718.1:c.77_78delinsCT	NP_001291647.1:p.Lys26Thr
XM_006717926.2:c.623_624delinsCT	XP_006717989.1:p.Lys208Thr
XM_011539981.1:c.668_669delinsCT	XP_011538283.1:p.Lys223Thr
XM_011539982.1:c.572_573delinsCT	XP_011538284.1:p.Lys191Thr
XR_945791.1:n.1238_1239delinsCT
NM_000314.7:c.668_669delinsCT	NP_000305.3:p.Lys223Thr
NM_001304717.5:c.1187_1188delinsCT	NP_001291646.4:p.Lys396Thr
NM_001304718.2:c.77_78delinsCT	NP_001291647.1:p.Lys26Thr
NM_000314.8:c.668_669delinsCT MANE Select	NP_000305.3:p.Lys223Thr