Canonical Allele Identifier: CA2791060478
Gene: PRR5L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350177_36350261del , CM000673.2:g.36350177_36350261del GRCh38
NC_000011.9:g.36371727_36371811del , CM000673.1:g.36371727_36371811del GRCh37
NC_000011.8:g.36328303_36328387del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50820_-125-50736del MANE Select ENSP00000435050.1:n.-125-50820_-125-50736del
ENST00000527172.5:c.-291-43669_-291-43585del ENSP00000433708.1:n.-291-43669_-291-43585del
ENST00000529034.5:n.152-50820_152-50736del
ENST00000530639.5:c.-125-50820_-125-50736del ENSP00000435050.1:n.-125-50820_-125-50736del
ENST00000532121.5:c.-126+112_-126+196del ENSP00000433893.1:n.-126+112_-126+196del
NM_001160167.1:c.-125-50820_-125-50736del NP_001153639.1:n.-125-50820_-125-50736del
NM_001160167.2:c.-125-50820_-125-50736del MANE Select NP_001153639.1:n.-125-50820_-125-50736del
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