Canonical Allele Identifier: CA669575001
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1386718227
MyVariant Identifiers: chr10:g.87967601T>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967601T>G , CM000672.2:g.87967601T>G GRCh38
NC_000010.10:g.89727358T>G , CM000672.1:g.89727358T>G GRCh37
NC_000010.9:g.89717338T>G NCBI36
NG_007466.2:g.109163T>G , LRG_311:g.109163T>G

Transcript Alleles

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