Canonical Allele Identifier: CA669540287

Linked Data

dbSNP Id: rs1447068304

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863367G>A , CM000672.2:g.87863367G>A GRCh38
NC_000010.10:g.89623124G>A , CM000672.1:g.89623124G>A GRCh37
NC_000010.9:g.89613104G>A NCBI36
NG_007466.2:g.4930G>A , LRG_311:g.4930G>A
NG_033079.1:g.5071C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000706954.1:c.-17+725G>A (PTEN) ENSP00000516674.1:n.-17+725G>A
ENST00000688308.1:c.-17+254G>A (PTEN) ENSP00000508752.1:n.-17+254G>A
ENST00000445946.5:c.-880C>T (KLLN) MANE Select ENSP00000392204.2:n.-880C>T
ENST00000371953.7:c.-1103G>A (PTEN) ENSP00000361021.3:n.-1103G>A
ENST00000445946.3:c.-880C>T (KLLN) ENSP00000392204.2:n.-880C>T
NM_001126049.1:c.-880C>T (KLLN) NP_001119521.1:n.-880C>T
NM_001126049.2:c.-880C>T (KLLN) MANE Select NP_001119521.1:n.-880C>T