Canonical Allele Identifier: CA2610045601

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863143C>A , CM000672.2:g.87863143C>A GRCh38
NC_000010.10:g.89622900C>A , CM000672.1:g.89622900C>A GRCh37
NC_000010.9:g.89612880C>A NCBI36
NG_007466.2:g.4706C>A , LRG_311:g.4706C>A
NG_033079.1:g.5295G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+501C>A (PTEN) ENSP00000516674.1:n.-17+501C>A
ENST00000688308.1:c.-17+30C>A (PTEN) ENSP00000508752.1:n.-17+30C>A
ENST00000445946.5:c.-656G>T (KLLN) MANE Select ENSP00000392204.2:n.-656G>T
ENST00000371953.7:c.-1327C>A (PTEN) ENSP00000361021.3:n.-1327C>A
ENST00000445946.3:c.-656G>T (KLLN) ENSP00000392204.2:n.-656G>T
NM_001126049.1:c.-656G>T (KLLN) NP_001119521.1:n.-656G>T
NM_001126049.2:c.-656G>T (KLLN) MANE Select NP_001119521.1:n.-656G>T