Canonical Allele Identifier: CA2582342713
Community Standard Title: NM_000314.8(PTEN):c.475delinsCTT (p.Arg159LeufsTer9)
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87933234delinsCTT , CM000672.2:g.87933234delinsCTT GRCh38
NC_000010.10:g.89692991delinsCTT , CM000672.1:g.89692991delinsCTT GRCh37
NC_000010.9:g.89682971delinsCTT NCBI36
NG_007466.2:g.74796delinsCTT , LRG_311:g.74796delinsCTT

Transcript Alleles

HGVS Amino-acid Change
NM_000314.8:c.475delinsCTT MANE Select NP_000305.3:p.Arg159LeufsTer9
ENST00000371953.8:c.475delinsCTT MANE Select ENSP00000361021.3:p.Arg159LeufsTer9
NM_000314.5:c.475delinsCTT NP_000305.3:p.Arg159LeufsTer9
NM_000314.6:c.475delinsCTT NP_000305.3:p.Arg159LeufsTer9
NM_000314.7:c.475delinsCTT NP_000305.3:p.Arg159LeufsTer9
NM_001304717.2:c.994delinsCTT NP_001291646.2:p.Arg332LeufsTer9
NM_001304717.5:c.994delinsCTT NP_001291646.4:p.Arg332LeufsTer9
NM_001304718.1:c.-276delinsCTT NP_001291647.1:n.-276delinsCTT
NM_001304718.2:c.-276delinsCTT NP_001291647.1:n.-276delinsCTT
ENST00000371953.7:c.475delinsCTT ENSP00000361021.3:p.Arg159LeufsTer9
ENST00000472832.3:c.475delinsCTT ENSP00000483066.2:p.Arg159LeufsTer9
ENST00000498703.1:n.301delinsCTT
ENST00000610634.1:c.373delinsCTT ENSP00000477517.1:p.Arg125LeufsTer22
ENST00000686459.1:c.475delinsCTT ENSP00000508909.1:p.Arg159LeufsTer22
ENST00000688158.1:c.*586delinsCTT ENSP00000509254.1:n.*586delinsCTT
ENST00000688158.2:n.1210delinsCTT
ENST00000688308.1:c.475delinsCTT ENSP00000508752.1:p.Arg159LeufsTer9
ENST00000688922.1:c.396delinsCTT
ENST00000688922.2:c.*305delinsCTT ENSP00000508742.2:n.*305delinsCTT
ENST00000693560.1:c.994delinsCTT ENSP00000509861.1:p.Arg332LeufsTer9
ENST00000700021.1:c.430delinsCTT ENSP00000514757.1:p.Arg144LeufsTer9
ENST00000700022.1:c.475delinsCTT ENSP00000514758.1:p.Arg159LeufsTer?
ENST00000700029.1:c.309delinsCTT
ENST00000700029.2:c.475delinsCTT ENSP00000514759.2:p.Arg159LeufsTer9
ENST00000706954.1:c.475delinsCTT ENSP00000516674.1:p.Arg159LeufsTer9
ENST00000706955.1:c.*510delinsCTT ENSP00000516675.1:n.*510delinsCTT
ENST00000710265.1:c.475delinsCTT ENSP00000518161.1:p.Arg159LeufsTer9
XM_006717926.2:c.430delinsCTT XP_006717989.1:p.Arg144LeufsTer9
XM_011539981.1:c.475delinsCTT XP_011538283.1:p.Arg159LeufsTer9
XM_011539982.1:c.379delinsCTT XP_011538284.1:p.Arg127LeufsTer9
XR_945789.1:n.1187delinsCTT
XR_945790.1:n.1187delinsCTT
XR_945791.1:n.1187delinsCTT