Canonical Allele Identifier: CA891838051
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965428_87965429delinsCC , CM000672.2:g.87965428_87965429delinsCC GRCh38
NC_000010.10:g.89725185_89725186delinsCC , CM000672.1:g.89725185_89725186delinsCC GRCh37
NC_000010.9:g.89715165_89715166delinsCC NCBI36
NG_007466.2:g.106990_106991delinsCC , LRG_311:g.106990_106991delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1261_1262delinsCC ENSP00000514759.2:p.Glu421Pro
ENST00000710265.1:c.*197_*198delinsCC ENSP00000518161.1:n.*197_*198delinsCC
ENST00000688158.2:n.1903_1904delinsCC
ENST00000688922.2:c.*998_*999delinsCC ENSP00000508742.2:n.*998_*999delinsCC
ENST00000700021.1:c.1123_1124delinsCC ENSP00000514757.1:p.Glu375Pro
ENST00000700022.1:c.*507_*508delinsCC ENSP00000514758.1:n.*507_*508delinsCC
ENST00000700023.1:n.2326_2327delinsCC
ENST00000700024.1:n.2560_2561delinsCC
ENST00000706954.1:c.1168_1169delinsCC ENSP00000516674.1:p.Glu390Pro
ENST00000706955.1:c.*1203_*1204delinsCC ENSP00000516675.1:n.*1203_*1204delinsCC
ENST00000686459.1:c.*754_*755delinsCC ENSP00000508909.1:n.*754_*755delinsCC
ENST00000688158.1:c.*1279_*1280delinsCC ENSP00000509254.1:n.*1279_*1280delinsCC
ENST00000688308.1:c.1168_1169delinsCC ENSP00000508752.1:p.Glu390Pro
ENST00000688922.1:c.1089_1090delinsCC
ENST00000693560.1:c.1687_1688delinsCC ENSP00000509861.1:p.Glu563Pro
ENST00000371953.8:c.1168_1169delinsCC MANE Select ENSP00000361021.3:p.Glu390Pro
ENST00000371953.7:c.1168_1169delinsCC ENSP00000361021.3:p.Glu390Pro
NM_000314.5:c.1168_1169delinsCC NP_000305.3:p.Glu390Pro
NM_000314.6:c.1168_1169delinsCC NP_000305.3:p.Glu390Pro
NM_001304717.2:c.1687_1688delinsCC NP_001291646.2:p.Glu563Pro
NM_001304718.1:c.577_578delinsCC NP_001291647.1:p.Glu193Pro
XM_006717926.2:c.1123_1124delinsCC XP_006717989.1:p.Glu375Pro
XM_011539982.1:c.1072_1073delinsCC XP_011538284.1:p.Glu358Pro
XR_945791.1:n.1738_1739delinsCC
NM_000314.7:c.1168_1169delinsCC NP_000305.3:p.Glu390Pro
NM_001304717.5:c.1687_1688delinsCC NP_001291646.4:p.Glu563Pro
NM_001304718.2:c.577_578delinsCC NP_001291647.1:p.Glu193Pro
NM_000314.8:c.1168_1169delinsCC MANE Select NP_000305.3:p.Glu390Pro