Canonical Allele Identifier: CA2613138621
Gene: PRR5L HGNC NCBI

Linked Data

gnomAD v4: 11-36350141-TGTGAGTGTGTGTGTGGGTGTGTGGGAGGGTGGGTGTGTGTGTGGGAGGGTGGGTGG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350145_36350200del , CM000673.2:g.36350145_36350200del GRCh38
NC_000011.9:g.36371695_36371750del , CM000673.1:g.36371695_36371750del GRCh37
NC_000011.8:g.36328271_36328326del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50852_-125-50797del MANE Select ENSP00000435050.1:n.-125-50852_-125-50797del
ENST00000527172.5:c.-291-43701_-291-43646del ENSP00000433708.1:n.-291-43701_-291-43646del
ENST00000529034.5:n.152-50852_152-50797del
ENST00000530639.5:c.-125-50852_-125-50797del ENSP00000435050.1:n.-125-50852_-125-50797del
ENST00000532121.5:c.-126+80_-126+135del ENSP00000433893.1:n.-126+80_-126+135del
NM_001160167.1:c.-125-50852_-125-50797del NP_001153639.1:n.-125-50852_-125-50797del
NM_001160167.2:c.-125-50852_-125-50797del MANE Select NP_001153639.1:n.-125-50852_-125-50797del
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