Canonical Allele Identifier: CA669540276

Linked Data

dbSNP Id: rs1250993282

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863362C>G , CM000672.2:g.87863362C>G GRCh38
NC_000010.10:g.89623119C>G , CM000672.1:g.89623119C>G GRCh37
NC_000010.9:g.89613099C>G NCBI36
NG_007466.2:g.4925C>G , LRG_311:g.4925C>G
NG_033079.1:g.5076G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+720C>G (PTEN) ENSP00000516674.1:n.-17+720C>G
ENST00000688308.1:c.-17+249C>G (PTEN) ENSP00000508752.1:n.-17+249C>G
ENST00000445946.5:c.-875G>C (KLLN) MANE Select ENSP00000392204.2:n.-875G>C
ENST00000371953.7:c.-1108C>G (PTEN) ENSP00000361021.3:n.-1108C>G
ENST00000445946.3:c.-875G>C (KLLN) ENSP00000392204.2:n.-875G>C
NM_001126049.1:c.-875G>C (KLLN) NP_001119521.1:n.-875G>C
NM_001126049.2:c.-875G>C (KLLN) MANE Select NP_001119521.1:n.-875G>C