Canonical Allele Identifier: CA211453352
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 440217
dbSNP Id: rs2943772

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87864144G>C , CM000672.2:g.87864144G>C GRCh38
NC_000010.10:g.89623901G>C , CM000672.1:g.89623901G>C GRCh37
NC_000010.9:g.89613881G>C NCBI36
NG_033079.1:g.4294C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.-326G>C ENSP00000514759.2:n.-326G>C
ENST00000710265.1:c.-326G>C ENSP00000518161.1:n.-326G>C
ENST00000700021.1:c.-326G>C ENSP00000514757.1:n.-326G>C
ENST00000700022.1:c.-326G>C ENSP00000514758.1:n.-326G>C
ENST00000706954.1:c.-16-310G>C ENSP00000516674.1:n.-16-310G>C
ENST00000706955.1:c.-326G>C ENSP00000516675.1:n.-326G>C
ENST00000688158.1:c.-326G>C ENSP00000509254.1:n.-326G>C
ENST00000688308.1:c.-16-310G>C ENSP00000508752.1:n.-16-310G>C
ENST00000693560.1:c.194G>C ENSP00000509861.1:p.Cys65Ser
ENST00000371953.8:c.-326G>C MANE Select ENSP00000361021.3:n.-326G>C
ENST00000371953.7:c.-326G>C ENSP00000361021.3:n.-326G>C
ENST00000610634.1:c.-428G>C ENSP00000477517.1:n.-428G>C
XM_006717926.2:c.-326G>C XP_006717989.1:n.-326G>C
XM_011539981.1:c.-326G>C XP_011538283.1:n.-326G>C
XR_945789.1:n.387G>C
XR_945790.1:n.387G>C
XR_945791.1:n.387G>C
NM_000314.8:c.-326G>C MANE Select NP_000305.3:n.-326G>C