Canonical Allele Identifier: CA891840097

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87958008_87958010delinsTTT , CM000672.2:g.87958008_87958010delinsTTT	GRCh38
NC_000010.10:g.89717765_89717767delinsTTT , CM000672.1:g.89717765_89717767delinsTTT	GRCh37
NC_000010.9:g.89707745_89707747delinsTTT	NCBI36
NG_007466.2:g.99570_99572delinsTTT , LRG_311:g.99570_99572delinsTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.790_792delinsTTT	ENSP00000514759.2:p.Met264Phe
ENST00000710265.1:c.790_792delinsTTT	ENSP00000518161.1:p.Met264Phe
ENST00000472832.3:c.790_792delinsTTT	ENSP00000483066.2:p.Met264Phe
ENST00000688158.2:n.1525_1527delinsTTT
ENST00000688922.2:c.*620_*622delinsTTT	ENSP00000508742.2:n.*620_*622delinsTTT
ENST00000700021.1:c.745_747delinsTTT	ENSP00000514757.1:p.Met249Phe
ENST00000700022.1:c.*129_*131delinsTTT	ENSP00000514758.1:n.*129_*131delinsTTT
ENST00000700023.1:n.1948_1950delinsTTT
ENST00000700024.1:n.2182_2184delinsTTT
ENST00000700025.1:n.1559_1561delinsTTT
ENST00000700026.1:n.427_429delinsTTT
ENST00000700029.1:c.624_626delinsTTT
ENST00000706954.1:c.790_792delinsTTT	ENSP00000516674.1:p.Met264Phe
ENST00000706955.1:c.*825_*827delinsTTT	ENSP00000516675.1:n.*825_*827delinsTTT
ENST00000686459.1:c.*376_*378delinsTTT	ENSP00000508909.1:n.*376_*378delinsTTT
ENST00000688158.1:c.*901_*903delinsTTT	ENSP00000509254.1:n.*901_*903delinsTTT
ENST00000688308.1:c.790_792delinsTTT	ENSP00000508752.1:p.Met264Phe
ENST00000688922.1:c.711_713delinsTTT
ENST00000693560.1:c.1309_1311delinsTTT	ENSP00000509861.1:p.Met437Phe
ENST00000371953.8:c.790_792delinsTTT MANE Select	ENSP00000361021.3:p.Met264Phe
ENST00000371953.7:c.790_792delinsTTT	ENSP00000361021.3:p.Met264Phe
ENST00000472832.2:c.217_219delinsTTT	ENSP00000483066.1:p.Met73Phe
NM_000314.5:c.790_792delinsTTT	NP_000305.3:p.Met264Phe
NM_000314.6:c.790_792delinsTTT	NP_000305.3:p.Met264Phe
NM_001304717.2:c.1309_1311delinsTTT	NP_001291646.2:p.Met437Phe
NM_001304718.1:c.199_201delinsTTT	NP_001291647.1:p.Met67Phe
XM_006717926.2:c.745_747delinsTTT	XP_006717989.1:p.Met249Phe
XM_011539981.1:c.790_792delinsTTT	XP_011538283.1:p.Met264Phe
XM_011539982.1:c.694_696delinsTTT	XP_011538284.1:p.Met232Phe
XR_945791.1:n.1360_1362delinsTTT
NM_000314.7:c.790_792delinsTTT	NP_000305.3:p.Met264Phe
NM_001304717.5:c.1309_1311delinsTTT	NP_001291646.4:p.Met437Phe
NM_001304718.2:c.199_201delinsTTT	NP_001291647.1:p.Met67Phe
NM_000314.8:c.790_792delinsTTT MANE Select	NP_000305.3:p.Met264Phe