Canonical Allele Identifier: CA2610045273

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863022dup , CM000672.2:g.87863022dup GRCh38
NC_000010.10:g.89622779dup , CM000672.1:g.89622779dup GRCh37
NC_000010.9:g.89612759dup NCBI36
NG_007466.2:g.4585dup , LRG_311:g.4585dup
NG_033079.1:g.5417dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+380dup (PTEN) ENSP00000516674.1:n.-17+380dup
ENST00000688308.1:c.-108dup (PTEN) ENSP00000508752.1:n.-108dup
ENST00000445946.5:c.-534dup (KLLN) MANE Select ENSP00000392204.2:n.-534dup
ENST00000445946.3:c.-534dup (KLLN) ENSP00000392204.2:n.-534dup
NM_001126049.1:c.-534dup (KLLN) NP_001119521.1:n.-534dup
NM_001126049.2:c.-534dup (KLLN) MANE Select NP_001119521.1:n.-534dup