Canonical Allele Identifier: CA891840100

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958009_87958010delinsCT , CM000672.2:g.87958009_87958010delinsCT	GRCh38
NC_000010.10:g.89717766_89717767delinsCT , CM000672.1:g.89717766_89717767delinsCT	GRCh37
NC_000010.9:g.89707746_89707747delinsCT	NCBI36
NG_007466.2:g.99571_99572delinsCT , LRG_311:g.99571_99572delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.791_792delinsCT	ENSP00000514759.2:p.Met264Thr
ENST00000710265.1:c.791_792delinsCT	ENSP00000518161.1:p.Met264Thr
ENST00000472832.3:c.791_792delinsCT	ENSP00000483066.2:p.Met264Thr
ENST00000688158.2:n.1526_1527delinsCT
ENST00000688922.2:c.*621_*622delinsCT	ENSP00000508742.2:n.*621_*622delinsCT
ENST00000700021.1:c.746_747delinsCT	ENSP00000514757.1:p.Met249Thr
ENST00000700022.1:c.*130_*131delinsCT	ENSP00000514758.1:n.*130_*131delinsCT
ENST00000700023.1:n.1949_1950delinsCT
ENST00000700024.1:n.2183_2184delinsCT
ENST00000700025.1:n.1560_1561delinsCT
ENST00000700026.1:n.428_429delinsCT
ENST00000700029.1:c.625_626delinsCT
ENST00000706954.1:c.791_792delinsCT	ENSP00000516674.1:p.Met264Thr
ENST00000706955.1:c.*826_*827delinsCT	ENSP00000516675.1:n.*826_*827delinsCT
ENST00000686459.1:c.*377_*378delinsCT	ENSP00000508909.1:n.*377_*378delinsCT
ENST00000688158.1:c.*902_*903delinsCT	ENSP00000509254.1:n.*902_*903delinsCT
ENST00000688308.1:c.791_792delinsCT	ENSP00000508752.1:p.Met264Thr
ENST00000688922.1:c.712_713delinsCT
ENST00000693560.1:c.1310_1311delinsCT	ENSP00000509861.1:p.Met437Thr
ENST00000371953.8:c.791_792delinsCT MANE Select	ENSP00000361021.3:p.Met264Thr
ENST00000371953.7:c.791_792delinsCT	ENSP00000361021.3:p.Met264Thr
ENST00000472832.2:c.218_219delinsCT	ENSP00000483066.1:p.Met73Thr
NM_000314.5:c.791_792delinsCT	NP_000305.3:p.Met264Thr
NM_000314.6:c.791_792delinsCT	NP_000305.3:p.Met264Thr
NM_001304717.2:c.1310_1311delinsCT	NP_001291646.2:p.Met437Thr
NM_001304718.1:c.200_201delinsCT	NP_001291647.1:p.Met67Thr
XM_006717926.2:c.746_747delinsCT	XP_006717989.1:p.Met249Thr
XM_011539981.1:c.791_792delinsCT	XP_011538283.1:p.Met264Thr
XM_011539982.1:c.695_696delinsCT	XP_011538284.1:p.Met232Thr
XR_945791.1:n.1361_1362delinsCT
NM_000314.7:c.791_792delinsCT	NP_000305.3:p.Met264Thr
NM_001304717.5:c.1310_1311delinsCT	NP_001291646.4:p.Met437Thr
NM_001304718.2:c.200_201delinsCT	NP_001291647.1:p.Met67Thr
NM_000314.8:c.791_792delinsCT MANE Select	NP_000305.3:p.Met264Thr