Canonical Allele Identifier: CA1926177048
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1860802918

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967632C>A , CM000672.2:g.87967632C>A GRCh38
NC_000010.10:g.89727389C>A , CM000672.1:g.89727389C>A GRCh37
NC_000010.9:g.89717369C>A NCBI36
NG_007466.2:g.109194C>A , LRG_311:g.109194C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000710265.1:c.*2401C>A ENSP00000518161.1:n.*2401C>A
ENST00000688158.2:n.4107C>A
ENST00000706954.1:c.*2160C>A ENSP00000516674.1:n.*2160C>A
ENST00000706955.1:c.*3407C>A ENSP00000516675.1:n.*3407C>A
ENST00000688158.1:c.*3483C>A ENSP00000509254.1:n.*3483C>A
ENST00000693560.1:c.*2160C>A ENSP00000509861.1:n.*2160C>A
ENST00000371953.8:c.*2160C>A MANE Select ENSP00000361021.3:n.*2160C>A
ENST00000371953.7:c.*2160C>A ENSP00000361021.3:n.*2160C>A
NM_000314.5:c.*2160C>A NP_000305.3:n.*2160C>A
NM_000314.6:c.*2160C>A NP_000305.3:n.*2160C>A
NM_001304717.2:c.*2160C>A NP_001291646.2:n.*2160C>A
NM_001304718.1:c.*2160C>A NP_001291647.1:n.*2160C>A
XM_006717926.2:c.*2160C>A XP_006717989.1:n.*2160C>A
XM_011539982.1:c.*2160C>A XP_011538284.1:n.*2160C>A
XR_945791.1:n.3942C>A
NM_000314.7:c.*2160C>A NP_000305.3:n.*2160C>A
NM_001304717.5:c.*2160C>A NP_001291646.4:n.*2160C>A
NM_001304718.2:c.*2160C>A NP_001291647.1:n.*2160C>A
NM_000314.8:c.*2160C>A MANE Select NP_000305.3:n.*2160C>A