Canonical Allele Identifier: CA2610045444

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863090C>T , CM000672.2:g.87863090C>T GRCh38
NC_000010.10:g.89622847C>T , CM000672.1:g.89622847C>T GRCh37
NC_000010.9:g.89612827C>T NCBI36
NG_007466.2:g.4653C>T , LRG_311:g.4653C>T
NG_033079.1:g.5348G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+448C>T (PTEN) ENSP00000516674.1:n.-17+448C>T
ENST00000688308.1:c.-40C>T (PTEN) ENSP00000508752.1:n.-40C>T
ENST00000445946.5:c.-603G>A (KLLN) MANE Select ENSP00000392204.2:n.-603G>A
ENST00000445946.3:c.-603G>A (KLLN) ENSP00000392204.2:n.-603G>A
NM_001126049.1:c.-603G>A (KLLN) NP_001119521.1:n.-603G>A
NM_001126049.2:c.-603G>A (KLLN) MANE Select NP_001119521.1:n.-603G>A