Canonical Allele Identifier: CA936880979
Gene: PRR5L HGNC NCBI

Linked Data

gnomAD v3: 11-36350141-TGTGAGTGTGTGTGTGGGTGTGTGGGAGGGTGGGTGTGTGTGTGGGAGGGTGGGTGGGTGTGAGTGTGTGTGGGGTGGGTGTGTGTGGGGGGTATAAGTGAGTGTGTGTGTGGGATGG-T
gnomAD v4: 11-36350141-TGTGAGTGTGTGTGTGGGTGTGTGGGAGGGTGGGTGTGTGTGTGGGAGGGTGGGTGGGTGTGAGTGTGTGTGGGGTGGGTGTGTGTGGGGGGTATAAGTGAGTGTGTGTGTGGGATGG-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350153_36350269del , CM000673.2:g.36350153_36350269del GRCh38
NC_000011.9:g.36371703_36371819del , CM000673.1:g.36371703_36371819del GRCh37
NC_000011.8:g.36328279_36328395del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50844_-125-50728del MANE Select ENSP00000435050.1:n.-125-50844_-125-50728...
ENST00000527172.5:c.-291-43693_-291-43577del ENSP00000433708.1:n.-291-43693_-291-43577...
ENST00000529034.5:n.152-50844_152-50728del
ENST00000530639.5:c.-125-50844_-125-50728del ENSP00000435050.1:n.-125-50844_-125-50728...
ENST00000532121.5:c.-126+88_-126+204del ENSP00000433893.1:n.-126+88_-126+204del
NM_001160167.1:c.-125-50844_-125-50728del NP_001153639.1:n.-125-50844_-125-50728del...
NM_001160167.2:c.-125-50844_-125-50728del MANE Select NP_001153639.1:n.-125-50844_-125-50728del...
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