Canonical Allele Identifier: CA645553740
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87925515_87933253del , CM000672.2:g.87925515_87933253del GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.167_492+2del
ENST00000710265.1:c.167_492+2del
ENST00000472832.3:c.167_492+2del
ENST00000688158.2:n.902_1227+2del
ENST00000688922.2:c.167_*322+2del
ENST00000700021.1:c.165-5531_447+2del
ENST00000700022.1:c.167_492+2del
ENST00000706954.1:c.167_492+2del
ENST00000706955.1:c.*202_*527+2del
ENST00000686459.1:c.167_492+2del
ENST00000688158.1:c.*278_*603+2del
ENST00000688308.1:c.167_492+2del
ENST00000688922.1:c.36_413+2del
ENST00000693560.1:c.686_1011+2del
ENST00000371953.8:c.167_492+2del
ENST00000371953.7:c.167_492+2del
ENST00000610634.1:c.65_390+2del
NM_000314.5:c.167_492+2del
NM_000314.6:c.167_492+2del
NM_001304717.2:c.686_1011+2del
NM_001304718.1:c.-541-5531_-259+2del
XM_006717926.2:c.165-5531_447+2del
XM_011539981.1:c.167_492+2del
XM_011539982.1:c.71_396+2del
XR_945789.1:n.879_1204+2del
XR_945790.1:n.879_1204+2del
XR_945791.1:n.879_1204+2del
NM_000314.7:c.167_492+2del
NM_001304717.5:c.686_1011+2del
NM_001304718.2:c.-541-5531_-259+2del
NM_000314.8:c.167_492+2del