Canonical Allele Identifier: CA891839909
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957972_87957974delinsAGA , CM000672.2:g.87957972_87957974delinsAGA GRCh38
NC_000010.10:g.89717729_89717731delinsAGA , CM000672.1:g.89717729_89717731delinsAGA GRCh37
NC_000010.9:g.89707709_89707711delinsAGA NCBI36
NG_007466.2:g.99534_99536delinsAGA , LRG_311:g.99534_99536delinsAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.754_756delinsAGA ENSP00000514759.2:p.Asp252Arg
ENST00000710265.1:c.754_756delinsAGA ENSP00000518161.1:p.Asp252Arg
ENST00000472832.3:c.754_756delinsAGA ENSP00000483066.2:p.Asp252Arg
ENST00000688158.2:n.1489_1491delinsAGA
ENST00000688922.2:c.*584_*586delinsAGA ENSP00000508742.2:n.*584_*586delinsAGA
ENST00000700021.1:c.709_711delinsAGA ENSP00000514757.1:p.Asp237Arg
ENST00000700022.1:c.*93_*95delinsAGA ENSP00000514758.1:n.*93_*95delinsAGA
ENST00000700023.1:n.1912_1914delinsAGA
ENST00000700024.1:n.2146_2148delinsAGA
ENST00000700025.1:n.1523_1525delinsAGA
ENST00000700026.1:n.391_393delinsAGA
ENST00000700029.1:c.588_590delinsAGA
ENST00000706954.1:c.754_756delinsAGA ENSP00000516674.1:p.Asp252Arg
ENST00000706955.1:c.*789_*791delinsAGA ENSP00000516675.1:n.*789_*791delinsAGA
ENST00000686459.1:c.*340_*342delinsAGA ENSP00000508909.1:n.*340_*342delinsAGA
ENST00000688158.1:c.*865_*867delinsAGA ENSP00000509254.1:n.*865_*867delinsAGA
ENST00000688308.1:c.754_756delinsAGA ENSP00000508752.1:p.Asp252Arg
ENST00000688922.1:c.675_677delinsAGA
ENST00000693560.1:c.1273_1275delinsAGA ENSP00000509861.1:p.Asp425Arg
ENST00000371953.8:c.754_756delinsAGA MANE Select ENSP00000361021.3:p.Asp252Arg
ENST00000371953.7:c.754_756delinsAGA ENSP00000361021.3:p.Asp252Arg
ENST00000472832.2:c.181_183delinsAGA ENSP00000483066.1:p.Asp61Arg
NM_000314.5:c.754_756delinsAGA NP_000305.3:p.Asp252Arg
NM_000314.6:c.754_756delinsAGA NP_000305.3:p.Asp252Arg
NM_001304717.2:c.1273_1275delinsAGA NP_001291646.2:p.Asp425Arg
NM_001304718.1:c.163_165delinsAGA NP_001291647.1:p.Asp55Arg
XM_006717926.2:c.709_711delinsAGA XP_006717989.1:p.Asp237Arg
XM_011539981.1:c.754_756delinsAGA XP_011538283.1:p.Asp252Arg
XM_011539982.1:c.658_660delinsAGA XP_011538284.1:p.Asp220Arg
XR_945791.1:n.1324_1326delinsAGA
NM_000314.7:c.754_756delinsAGA NP_000305.3:p.Asp252Arg
NM_001304717.5:c.1273_1275delinsAGA NP_001291646.4:p.Asp425Arg
NM_001304718.2:c.163_165delinsAGA NP_001291647.1:p.Asp55Arg
NM_000314.8:c.754_756delinsAGA MANE Select NP_000305.3:p.Asp252Arg