Canonical Allele Identifier: CA1926177404
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1860809456

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967873_87967882del , CM000672.2:g.87967873_87967882del GRCh38
NC_000010.10:g.89727630_89727639del , CM000672.1:g.89727630_89727639del GRCh37
NC_000010.9:g.89717610_89717619del NCBI36
NG_007466.2:g.109435_109444del , LRG_311:g.109435_109444del

Transcript Alleles

HGVS Amino-acid Change
ENST00000710265.1:c.*2642_*2651del ENSP00000518161.1:n.*2642_*2651del
ENST00000688158.2:n.4348_4357del
ENST00000706954.1:c.*2401_*2410del ENSP00000516674.1:n.*2401_*2410del
ENST00000706955.1:c.*3648_*3657del ENSP00000516675.1:n.*3648_*3657del
ENST00000688158.1:c.*3724_*3733del ENSP00000509254.1:n.*3724_*3733del
ENST00000693560.1:c.*2401_*2410del ENSP00000509861.1:n.*2401_*2410del
ENST00000371953.8:c.*2401_*2410del MANE Select ENSP00000361021.3:n.*2401_*2410del
ENST00000371953.7:c.*2401_*2410del ENSP00000361021.3:n.*2401_*2410del
NM_000314.5:c.*2401_*2410del NP_000305.3:n.*2401_*2410del
NM_000314.6:c.*2401_*2410del NP_000305.3:n.*2401_*2410del
NM_001304717.2:c.*2401_*2410del NP_001291646.2:n.*2401_*2410del
NM_001304718.1:c.*2401_*2410del NP_001291647.1:n.*2401_*2410del
XM_006717926.2:c.*2401_*2410del XP_006717989.1:n.*2401_*2410del
XM_011539982.1:c.*2401_*2410del XP_011538284.1:n.*2401_*2410del
XR_945791.1:n.4183_4192del
NM_000314.7:c.*2401_*2410del NP_000305.3:n.*2401_*2410del
NM_001304717.5:c.*2401_*2410del NP_001291646.4:n.*2401_*2410del
NM_001304718.2:c.*2401_*2410del NP_001291647.1:n.*2401_*2410del
NM_000314.8:c.*2401_*2410del MANE Select NP_000305.3:n.*2401_*2410del