Canonical Allele Identifier: CA2722432827
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132277824

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958014_87958020del , CM000672.2:g.87958014_87958020del GRCh38
NC_000010.10:g.89717771_89717777del , CM000672.1:g.89717771_89717777del GRCh37
NC_000010.9:g.89707751_89707757del NCBI36
NG_007466.2:g.99576_99582del , LRG_311:g.99576_99582del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.796_801+1del
ENST00000710265.1:c.796_801+1del
ENST00000472832.3:c.796_801+1del
ENST00000688158.2:n.1531_1536+1del
ENST00000688922.2:c.*626_*631+1del
ENST00000700021.1:c.751_756+1del
ENST00000700022.1:c.*135_*140+1del
ENST00000700023.1:n.1954_1959+1del
ENST00000700024.1:n.2188_2193+1del
ENST00000700025.1:n.1565_1570+1del
ENST00000700026.1:n.433_438+1del
ENST00000700029.1:c.630_635+1del
ENST00000706954.1:c.796_801+1del
ENST00000706955.1:c.*831_*836+1del
ENST00000686459.1:c.*382_*387+1del
ENST00000688158.1:c.*907_*912+1del
ENST00000688308.1:c.796_801+1del
ENST00000688922.1:c.717_722+1del
ENST00000693560.1:c.1315_1320+1del
ENST00000371953.8:c.796_801+1del
ENST00000371953.7:c.796_801+1del
ENST00000472832.2:c.223_228+1del
NM_000314.5:c.796_801+1del
NM_000314.6:c.796_801+1del
NM_001304717.2:c.1315_1320+1del
NM_001304718.1:c.205_210+1del
XM_006717926.2:c.751_756+1del
XM_011539981.1:c.796_801+1del
XM_011539982.1:c.700_705+1del
XR_945791.1:n.1366_1371+1del
NM_000314.7:c.796_801+1del
NM_001304717.5:c.1315_1320+1del
NM_001304718.2:c.205_210+1del
NM_000314.8:c.796_801+1del