Canonical Allele Identifier: CA2613138604
Gene: PRR5L HGNC NCBI

Linked Data

gnomAD v4: 11-36350129-AGTGAGTGTGTGTGTGAGTGTGTGTGTGGGTGTGTGGGAGGGTGGGTGTGTGTGTGGGAGGGTGGGTGGGTGTGAGTGTGTGTGGGGTGGGTGTGTGTGGGGGGTATAAGTGAGTGTGTGTGTGGGATGG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350141_36350269del , CM000673.2:g.36350141_36350269del GRCh38
NC_000011.9:g.36371691_36371819del , CM000673.1:g.36371691_36371819del GRCh37
NC_000011.8:g.36328267_36328395del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50856_-125-50728del MANE Select ENSP00000435050.1:n.-125-50856_-125-50728del
ENST00000527172.5:c.-291-43705_-291-43577del ENSP00000433708.1:n.-291-43705_-291-43577del
ENST00000529034.5:n.152-50856_152-50728del
ENST00000530639.5:c.-125-50856_-125-50728del ENSP00000435050.1:n.-125-50856_-125-50728del
ENST00000532121.5:c.-126+76_-126+204del ENSP00000433893.1:n.-126+76_-126+204del
NM_001160167.1:c.-125-50856_-125-50728del NP_001153639.1:n.-125-50856_-125-50728del
NM_001160167.2:c.-125-50856_-125-50728del MANE Select NP_001153639.1:n.-125-50856_-125-50728del
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