Canonical Allele Identifier: CA2610045388

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87863063del , CM000672.2:g.87863063del GRCh38
NC_000010.10:g.89622820del , CM000672.1:g.89622820del GRCh37
NC_000010.9:g.89612800del NCBI36
NG_007466.2:g.4626del , LRG_311:g.4626del
NG_033079.1:g.5377del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706954.1:c.-17+421del (PTEN) ENSP00000516674.1:n.-17+421del
ENST00000688308.1:c.-67del (PTEN) ENSP00000508752.1:n.-67del
ENST00000445946.5:c.-574del (KLLN) MANE Select ENSP00000392204.2:n.-574del
ENST00000445946.3:c.-574del (KLLN) ENSP00000392204.2:n.-574del
NM_001126049.1:c.-574del (KLLN) NP_001119521.1:n.-574del
NM_001126049.2:c.-574del (KLLN) MANE Select NP_001119521.1:n.-574del