Canonical Allele Identifier: CA2613138607
Gene: PRR5L HGNC NCBI

Linked Data

gnomAD v4: 11-36350131-TGA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350133_36350134del , CM000673.2:g.36350133_36350134del GRCh38
NC_000011.9:g.36371683_36371684del , CM000673.1:g.36371683_36371684del GRCh37
NC_000011.8:g.36328259_36328260del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50864_-125-50863del MANE Select ENSP00000435050.1:n.-125-50864_-125-50863del
ENST00000527172.5:c.-291-43713_-291-43712del ENSP00000433708.1:n.-291-43713_-291-43712del
ENST00000529034.5:n.152-50864_152-50863del
ENST00000530639.5:c.-125-50864_-125-50863del ENSP00000435050.1:n.-125-50864_-125-50863del
ENST00000532121.5:c.-126+68_-126+69del ENSP00000433893.1:n.-126+68_-126+69del
NM_001160167.1:c.-125-50864_-125-50863del NP_001153639.1:n.-125-50864_-125-50863del
NM_001160167.2:c.-125-50864_-125-50863del MANE Select NP_001153639.1:n.-125-50864_-125-50863del
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