Canonical Allele Identifier: CA595073162

Linked Data

ClinVar Variation Id: 488905
ClinVar RCV Id: RCV000579323
dbSNP Id: rs1173886666

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863148C>A , CM000672.2:g.87863148C>A GRCh38
NC_000010.10:g.89622905C>A , CM000672.1:g.89622905C>A GRCh37
NC_000010.9:g.89612885C>A NCBI36
NG_007466.2:g.4711C>A , LRG_311:g.4711C>A
NG_033079.1:g.5290G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+506C>A (PTEN) ENSP00000516674.1:n.-17+506C>A
ENST00000688308.1:c.-17+35C>A (PTEN) ENSP00000508752.1:n.-17+35C>A
ENST00000445946.5:c.-661G>T (KLLN) MANE Select ENSP00000392204.2:n.-661G>T
ENST00000371953.7:c.-1322C>A (PTEN) ENSP00000361021.3:n.-1322C>A
ENST00000445946.3:c.-661G>T (KLLN) ENSP00000392204.2:n.-661G>T
NM_001126049.1:c.-661G>T (KLLN) NP_001119521.1:n.-661G>T
NM_001126049.2:c.-661G>T (KLLN) MANE Select NP_001119521.1:n.-661G>T