Canonical Allele Identifier: CA1926143090
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1589594090

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863547C>G , CM000672.2:g.87863547C>G GRCh38
NC_000010.10:g.89623304C>G , CM000672.1:g.89623304C>G GRCh37
NC_000010.9:g.89613284C>G NCBI36
NG_007466.2:g.5110C>G , LRG_311:g.5110C>G
NG_033079.1:g.4891G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000706954.1:c.-17+905C>G ENSP00000516674.1:n.-17+905C>G
ENST00000688308.1:c.-17+434C>G ENSP00000508752.1:n.-17+434C>G
ENST00000693560.1:c.-403C>G ENSP00000509861.1:n.-403C>G
ENST00000371953.7:c.-923C>G ENSP00000361021.3:n.-923C>G
ENST00000610634.1:c.-1025C>G ENSP00000477517.1:n.-1025C>G
NM_000314.5:c.-922C>G NP_000305.3:n.-922C>G
NM_000314.6:c.-922C>G NP_000305.3:n.-922C>G
NM_001304717.2:c.-403C>G NP_001291646.2:n.-403C>G
NM_001304718.1:c.-1627C>G NP_001291647.1:n.-1627C>G