Canonical Allele Identifier: CA1926142862

Linked Data

dbSNP Id: rs1589593637

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863302G>C , CM000672.2:g.87863302G>C GRCh38
NC_000010.10:g.89623059G>C , CM000672.1:g.89623059G>C GRCh37
NC_000010.9:g.89613039G>C NCBI36
NG_007466.2:g.4865G>C , LRG_311:g.4865G>C
NG_033079.1:g.5136C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+660G>C (PTEN) ENSP00000516674.1:n.-17+660G>C
ENST00000688308.1:c.-17+189G>C (PTEN) ENSP00000508752.1:n.-17+189G>C
ENST00000445946.5:c.-815C>G (KLLN) MANE Select ENSP00000392204.2:n.-815C>G
ENST00000371953.7:c.-1168G>C (PTEN) ENSP00000361021.3:n.-1168G>C
ENST00000445946.3:c.-815C>G (KLLN) ENSP00000392204.2:n.-815C>G
NM_001126049.1:c.-815C>G (KLLN) NP_001119521.1:n.-815C>G
NM_001126049.2:c.-815C>G (KLLN) MANE Select NP_001119521.1:n.-815C>G