Canonical Allele Identifier: CA10636417
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 301463
ClinVar RCV Id: RCV000301364
dbSNP Id: rs701848

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87966988T>C , CM000672.2:g.87966988T>C GRCh38
NC_000010.10:g.89726745T>C , CM000672.1:g.89726745T>C GRCh37
NC_000010.9:g.89716725T>C NCBI36
NG_007466.2:g.108550T>C , LRG_311:g.108550T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000710265.1:c.*1757T>C ENSP00000518161.1:n.*1757T>C
ENST00000688158.2:n.3463T>C
ENST00000706954.1:c.*1516T>C ENSP00000516674.1:n.*1516T>C
ENST00000706955.1:c.*2763T>C ENSP00000516675.1:n.*2763T>C
ENST00000688158.1:c.*2839T>C ENSP00000509254.1:n.*2839T>C
ENST00000693560.1:c.*1516T>C ENSP00000509861.1:n.*1516T>C
ENST00000371953.8:c.*1516T>C MANE Select ENSP00000361021.3:n.*1516T>C
ENST00000371953.7:c.*1516T>C ENSP00000361021.3:n.*1516T>C
NM_000314.5:c.*1516T>C NP_000305.3:n.*1516T>C
NM_000314.6:c.*1516T>C NP_000305.3:n.*1516T>C
NM_001304717.2:c.*1516T>C NP_001291646.2:n.*1516T>C
NM_001304718.1:c.*1516T>C NP_001291647.1:n.*1516T>C
XM_006717926.2:c.*1516T>C XP_006717989.1:n.*1516T>C
XM_011539982.1:c.*1516T>C XP_011538284.1:n.*1516T>C
XR_945791.1:n.3298T>C
NM_000314.7:c.*1516T>C NP_000305.3:n.*1516T>C
NM_001304717.5:c.*1516T>C NP_001291646.4:n.*1516T>C
NM_001304718.2:c.*1516T>C NP_001291647.1:n.*1516T>C
NM_000314.8:c.*1516T>C MANE Select NP_000305.3:n.*1516T>C