Canonical Allele Identifier: CA2579927071
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894108_87894110delinsTAA , CM000672.2:g.87894108_87894110delinsTAA GRCh38
NC_000010.10:g.89653865_89653867delinsTAA , CM000672.1:g.89653865_89653867delinsTAA GRCh37
NC_000010.9:g.89643845_89643847delinsTAA NCBI36
NG_007466.2:g.35670_35672delinsTAA , LRG_311:g.35670_35672delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.163_164+1delinsTAA
ENST00000710265.1:c.163_164+1delinsTAA
ENST00000472832.3:c.163_164+1delinsTAA
ENST00000688158.2:n.899+13670_899+13672delinsTAA
ENST00000688922.2:c.163_164+1delinsTAA
ENST00000700021.1:c.163_164+1delinsTAA
ENST00000700022.1:c.163_164+1delinsTAA
ENST00000706954.1:c.163_164+1delinsTAA
ENST00000706955.1:c.*198_*199+1delinsTAA
ENST00000686459.1:c.163_164+1delinsTAA
ENST00000688158.1:c.*275+13670_*275+13672delinsTAA ENSP00000509254.1:n.*275+13670_*275+13672delinsTAA
ENST00000688308.1:c.163_164+1delinsTAA
ENST00000688922.1:c.32_33+1delinsTAA
ENST00000693560.1:c.682_683+1delinsTAA
ENST00000371953.8:c.163_164+1delinsTAA
ENST00000371953.7:c.163_164+1delinsTAA
ENST00000462694.1:n.165_167delinsTAA
ENST00000610634.1:c.61_62+1delinsTAA
NM_000314.5:c.163_164+1delinsTAA
NM_000314.6:c.163_164+1delinsTAA
NM_001304717.2:c.682_683+1delinsTAA
NM_001304718.1:c.-543_-542+1delinsTAA
XM_006717926.2:c.163_164+1delinsTAA
XM_011539981.1:c.163_164+1delinsTAA
XM_011539982.1:c.68+13670_68+13672delinsTAA XP_011538284.1:n.68+13670_68+13672delinsTAA
XR_945789.1:n.875_876+1delinsTAA
XR_945790.1:n.875_876+1delinsTAA
XR_945791.1:n.875_876+1delinsTAA
NM_000314.7:c.163_164+1delinsTAA
NM_001304717.5:c.682_683+1delinsTAA
NM_001304718.2:c.-543_-542+1delinsTAA
NM_000314.8:c.163_164+1delinsTAA