Canonical Allele Identifier: CA891839948

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957979_87957980delinsCT , CM000672.2:g.87957979_87957980delinsCT	GRCh38
NC_000010.10:g.89717736_89717737delinsCT , CM000672.1:g.89717736_89717737delinsCT	GRCh37
NC_000010.9:g.89707716_89707717delinsCT	NCBI36
NG_007466.2:g.99541_99542delinsCT , LRG_311:g.99541_99542delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.761_762delinsCT	ENSP00000514759.2:p.Lys254Thr
ENST00000710265.1:c.761_762delinsCT	ENSP00000518161.1:p.Lys254Thr
ENST00000472832.3:c.761_762delinsCT	ENSP00000483066.2:p.Lys254Thr
ENST00000688158.2:n.1496_1497delinsCT
ENST00000688922.2:c.*591_*592delinsCT	ENSP00000508742.2:n.*591_*592delinsCT
ENST00000700021.1:c.716_717delinsCT	ENSP00000514757.1:p.Lys239Thr
ENST00000700022.1:c.*100_*101delinsCT	ENSP00000514758.1:n.*100_*101delinsCT
ENST00000700023.1:n.1919_1920delinsCT
ENST00000700024.1:n.2153_2154delinsCT
ENST00000700025.1:n.1530_1531delinsCT
ENST00000700026.1:n.398_399delinsCT
ENST00000700029.1:c.595_596delinsCT
ENST00000706954.1:c.761_762delinsCT	ENSP00000516674.1:p.Lys254Thr
ENST00000706955.1:c.*796_*797delinsCT	ENSP00000516675.1:n.*796_*797delinsCT
ENST00000686459.1:c.*347_*348delinsCT	ENSP00000508909.1:n.*347_*348delinsCT
ENST00000688158.1:c.*872_*873delinsCT	ENSP00000509254.1:n.*872_*873delinsCT
ENST00000688308.1:c.761_762delinsCT	ENSP00000508752.1:p.Lys254Thr
ENST00000688922.1:c.682_683delinsCT
ENST00000693560.1:c.1280_1281delinsCT	ENSP00000509861.1:p.Lys427Thr
ENST00000371953.8:c.761_762delinsCT MANE Select	ENSP00000361021.3:p.Lys254Thr
ENST00000371953.7:c.761_762delinsCT	ENSP00000361021.3:p.Lys254Thr
ENST00000472832.2:c.188_189delinsCT	ENSP00000483066.1:p.Lys63Thr
NM_000314.5:c.761_762delinsCT	NP_000305.3:p.Lys254Thr
NM_000314.6:c.761_762delinsCT	NP_000305.3:p.Lys254Thr
NM_001304717.2:c.1280_1281delinsCT	NP_001291646.2:p.Lys427Thr
NM_001304718.1:c.170_171delinsCT	NP_001291647.1:p.Lys57Thr
XM_006717926.2:c.716_717delinsCT	XP_006717989.1:p.Lys239Thr
XM_011539981.1:c.761_762delinsCT	XP_011538283.1:p.Lys254Thr
XM_011539982.1:c.665_666delinsCT	XP_011538284.1:p.Lys222Thr
XR_945791.1:n.1331_1332delinsCT
NM_000314.7:c.761_762delinsCT	NP_000305.3:p.Lys254Thr
NM_001304717.5:c.1280_1281delinsCT	NP_001291646.4:p.Lys427Thr
NM_001304718.2:c.170_171delinsCT	NP_001291647.1:p.Lys57Thr
NM_000314.8:c.761_762delinsCT MANE Select	NP_000305.3:p.Lys254Thr