Canonical Allele Identifier: CA1926188623
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958012_87958020delinsTAAAAAAGG , CM000672.2:g.87958012_87958020delinsTAAAAAAGG GRCh38
NC_000010.10:g.89717769_89717777delinsTAAAAAAGG , CM000672.1:g.89717769_89717777delinsTAAAAAAGG GRCh37
NC_000010.9:g.89707749_89707757delinsTAAAAAAGG NCBI36
NG_007466.2:g.99574_99582delinsTAAAAAAGG , LRG_311:g.99574_99582delinsTAAAAAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.794_801+1delinsTAAAAAAGG
ENST00000710265.1:c.794_801+1delinsTAAAAAAGG
ENST00000472832.3:c.794_801+1delinsTAAAAAAGG
ENST00000688158.2:n.1529_1536+1delinsTAAAAAAGG
ENST00000688922.2:c.*624_*631+1delinsTAAAAAAGG
ENST00000700021.1:c.749_756+1delinsTAAAAAAGG
ENST00000700022.1:c.*133_*140+1delinsTAAAAAAGG
ENST00000700023.1:n.1952_1959+1delinsTAAAAAAGG
ENST00000700024.1:n.2186_2193+1delinsTAAAAAAGG
ENST00000700025.1:n.1563_1570+1delinsTAAAAAAGG
ENST00000700026.1:n.431_438+1delinsTAAAAAAGG
ENST00000700029.1:c.628_635+1delinsTAAAAAAGG
ENST00000706954.1:c.794_801+1delinsTAAAAAAGG
ENST00000706955.1:c.*829_*836+1delinsTAAAAAAGG
ENST00000686459.1:c.*380_*387+1delinsTAAAAAAGG
ENST00000688158.1:c.*905_*912+1delinsTAAAAAAGG
ENST00000688308.1:c.794_801+1delinsTAAAAAAGG
ENST00000688922.1:c.715_722+1delinsTAAAAAAGG
ENST00000693560.1:c.1313_1320+1delinsTAAAAAAGG
ENST00000371953.8:c.794_801+1delinsTAAAAAAGG
ENST00000371953.7:c.794_801+1delinsTAAAAAAGG
ENST00000472832.2:c.221_228+1delinsTAAAAAAGG
NM_000314.5:c.794_801+1delinsTAAAAAAGG
NM_000314.6:c.794_801+1delinsTAAAAAAGG
NM_001304717.2:c.1313_1320+1delinsTAAAAAAGG
NM_001304718.1:c.203_210+1delinsTAAAAAAGG
XM_006717926.2:c.749_756+1delinsTAAAAAAGG
XM_011539981.1:c.794_801+1delinsTAAAAAAGG
XM_011539982.1:c.698_705+1delinsTAAAAAAGG
XR_945791.1:n.1364_1371+1delinsTAAAAAAGG
NM_000314.7:c.794_801+1delinsTAAAAAAGG
NM_001304717.5:c.1313_1320+1delinsTAAAAAAGG
NM_001304718.2:c.203_210+1delinsTAAAAAAGG
NM_000314.8:c.794_801+1delinsTAAAAAAGG