Canonical Allele Identifier: CA2610045279

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863022A>C , CM000672.2:g.87863022A>C GRCh38
NC_000010.10:g.89622779A>C , CM000672.1:g.89622779A>C GRCh37
NC_000010.9:g.89612759A>C NCBI36
NG_007466.2:g.4585A>C , LRG_311:g.4585A>C
NG_033079.1:g.5416T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+380A>C (PTEN) ENSP00000516674.1:n.-17+380A>C
ENST00000688308.1:c.-108A>C (PTEN) ENSP00000508752.1:n.-108A>C
ENST00000445946.5:c.-535T>G (KLLN) MANE Select ENSP00000392204.2:n.-535T>G
ENST00000445946.3:c.-535T>G (KLLN) ENSP00000392204.2:n.-535T>G
NM_001126049.1:c.-535T>G (KLLN) NP_001119521.1:n.-535T>G
NM_001126049.2:c.-535T>G (KLLN) MANE Select NP_001119521.1:n.-535T>G