Canonical Allele Identifier: CA1926176835
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1860799381

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967510_87967514del , CM000672.2:g.87967510_87967514del GRCh38
NC_000010.10:g.89727267_89727271del , CM000672.1:g.89727267_89727271del GRCh37
NC_000010.9:g.89717247_89717251del NCBI36
NG_007466.2:g.109072_109076del , LRG_311:g.109072_109076del

Transcript Alleles

HGVS Amino-acid change
ENST00000710265.1:c.*2279_*2283del ENSP00000518161.1:n.*2279_*2283del
ENST00000688158.2:n.3985_3989del
ENST00000706954.1:c.*2038_*2042del ENSP00000516674.1:n.*2038_*2042del
ENST00000706955.1:c.*3285_*3289del ENSP00000516675.1:n.*3285_*3289del
ENST00000688158.1:c.*3361_*3365del ENSP00000509254.1:n.*3361_*3365del
ENST00000693560.1:c.*2038_*2042del ENSP00000509861.1:n.*2038_*2042del
ENST00000371953.8:c.*2038_*2042del MANE Select ENSP00000361021.3:n.*2038_*2042del
ENST00000371953.7:c.*2038_*2042del ENSP00000361021.3:n.*2038_*2042del
NM_000314.5:c.*2038_*2042del NP_000305.3:n.*2038_*2042del
NM_000314.6:c.*2038_*2042del NP_000305.3:n.*2038_*2042del
NM_001304717.2:c.*2038_*2042del NP_001291646.2:n.*2038_*2042del
NM_001304718.1:c.*2038_*2042del NP_001291647.1:n.*2038_*2042del
XM_006717926.2:c.*2038_*2042del XP_006717989.1:n.*2038_*2042del
XM_011539982.1:c.*2038_*2042del XP_011538284.1:n.*2038_*2042del
XR_945791.1:n.3820_3824del
NM_000314.7:c.*2038_*2042del NP_000305.3:n.*2038_*2042del
NM_001304717.5:c.*2038_*2042del NP_001291646.4:n.*2038_*2042del
NM_001304718.2:c.*2038_*2042del NP_001291647.1:n.*2038_*2042del
NM_000314.8:c.*2038_*2042del MANE Select NP_000305.3:n.*2038_*2042del