Canonical Allele Identifier: CA1926177421
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1860809714

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967878_87967886dup , CM000672.2:g.87967878_87967886dup GRCh38
NC_000010.10:g.89727635_89727643dup , CM000672.1:g.89727635_89727643dup GRCh37
NC_000010.9:g.89717615_89717623dup NCBI36
NG_007466.2:g.109440_109448dup , LRG_311:g.109440_109448dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000710265.1:c.*2647_*2655dup ENSP00000518161.1:n.*2647_*2655dup
ENST00000688158.2:n.4353_4361dup
ENST00000706954.1:c.*2406_*2414dup ENSP00000516674.1:n.*2406_*2414dup
ENST00000706955.1:c.*3653_*3661dup ENSP00000516675.1:n.*3653_*3661dup
ENST00000688158.1:c.*3729_*3737dup ENSP00000509254.1:n.*3729_*3737dup
ENST00000693560.1:c.*2406_*2414dup ENSP00000509861.1:n.*2406_*2414dup
ENST00000371953.8:c.*2406_*2414dup MANE Select ENSP00000361021.3:n.*2406_*2414dup
ENST00000371953.7:c.*2406_*2414dup ENSP00000361021.3:n.*2406_*2414dup
NM_000314.5:c.*2406_*2414dup NP_000305.3:n.*2406_*2414dup
NM_000314.6:c.*2406_*2414dup NP_000305.3:n.*2406_*2414dup
NM_001304717.2:c.*2406_*2414dup NP_001291646.2:n.*2406_*2414dup
NM_001304718.1:c.*2406_*2414dup NP_001291647.1:n.*2406_*2414dup
XM_006717926.2:c.*2406_*2414dup XP_006717989.1:n.*2406_*2414dup
XM_011539982.1:c.*2406_*2414dup XP_011538284.1:n.*2406_*2414dup
XR_945791.1:n.4188_4196dup
NM_000314.7:c.*2406_*2414dup NP_000305.3:n.*2406_*2414dup
NM_001304717.5:c.*2406_*2414dup NP_001291646.4:n.*2406_*2414dup
NM_001304718.2:c.*2406_*2414dup NP_001291647.1:n.*2406_*2414dup
NM_000314.8:c.*2406_*2414dup MANE Select NP_000305.3:n.*2406_*2414dup