Canonical Allele Identifier: CA669575002
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1322129546

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967601_87967602dup , CM000672.2:g.87967601_87967602dup GRCh38
NC_000010.10:g.89727358_89727359dup , CM000672.1:g.89727358_89727359dup GRCh37
NC_000010.9:g.89717338_89717339dup NCBI36
NG_007466.2:g.109163_109164dup , LRG_311:g.109163_109164dup

Transcript Alleles

HGVS Amino-acid change
ENST00000710265.1:c.*2370_*2371dup ENSP00000518161.1:n.*2370_*2371dup
ENST00000688158.2:n.4076_4077dup
ENST00000706954.1:c.*2129_*2130dup ENSP00000516674.1:n.*2129_*2130dup
ENST00000706955.1:c.*3376_*3377dup ENSP00000516675.1:n.*3376_*3377dup
ENST00000688158.1:c.*3452_*3453dup ENSP00000509254.1:n.*3452_*3453dup
ENST00000693560.1:c.*2129_*2130dup ENSP00000509861.1:n.*2129_*2130dup
ENST00000371953.8:c.*2129_*2130dup MANE Select ENSP00000361021.3:n.*2129_*2130dup
ENST00000371953.7:c.*2129_*2130dup ENSP00000361021.3:n.*2129_*2130dup
NM_000314.5:c.*2129_*2130dup NP_000305.3:n.*2129_*2130dup
NM_000314.6:c.*2129_*2130dup NP_000305.3:n.*2129_*2130dup
NM_001304717.2:c.*2129_*2130dup NP_001291646.2:n.*2129_*2130dup
NM_001304718.1:c.*2129_*2130dup NP_001291647.1:n.*2129_*2130dup
XM_006717926.2:c.*2129_*2130dup XP_006717989.1:n.*2129_*2130dup
XM_011539982.1:c.*2129_*2130dup XP_011538284.1:n.*2129_*2130dup
XR_945791.1:n.3911_3912dup
NM_000314.7:c.*2129_*2130dup NP_000305.3:n.*2129_*2130dup
NM_001304717.5:c.*2129_*2130dup NP_001291646.4:n.*2129_*2130dup
NM_001304718.2:c.*2129_*2130dup NP_001291647.1:n.*2129_*2130dup
NM_000314.8:c.*2129_*2130dup MANE Select NP_000305.3:n.*2129_*2130dup