Canonical Allele Identifier: CA669540019

Linked Data

dbSNP Id: rs1359211064

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863121C>G , CM000672.2:g.87863121C>G GRCh38
NC_000010.10:g.89622878C>G , CM000672.1:g.89622878C>G GRCh37
NC_000010.9:g.89612858C>G NCBI36
NG_007466.2:g.4684C>G , LRG_311:g.4684C>G
NG_033079.1:g.5317G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+479C>G (PTEN) ENSP00000516674.1:n.-17+479C>G
ENST00000688308.1:c.-17+8C>G (PTEN) ENSP00000508752.1:n.-17+8C>G
ENST00000445946.5:c.-634G>C (KLLN) MANE Select ENSP00000392204.2:n.-634G>C
ENST00000371953.7:c.-1349C>G (PTEN) ENSP00000361021.3:n.-1349C>G
ENST00000445946.3:c.-634G>C (KLLN) ENSP00000392204.2:n.-634G>C
NM_001126049.1:c.-634G>C (KLLN) NP_001119521.1:n.-634G>C
NM_001126049.2:c.-634G>C (KLLN) MANE Select NP_001119521.1:n.-634G>C