Canonical Allele Identifier: CA936881018
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1856912391
gnomAD v3: 11-36350167-AGGGTGGGTGTGTGTGTGGGAGGGTGGGTGGGTGTGAGTGTGTGTGGGGTGGGTGTGTGT-A
gnomAD v4: 11-36350167-AGGGTGGGTGTGTGTGTGGGAGGGTGGGTGGGTGTGAGTGTGTGTGGGGTGGGTGTGTGT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350171_36350229del , CM000673.2:g.36350171_36350229del GRCh38
NC_000011.9:g.36371721_36371779del , CM000673.1:g.36371721_36371779del GRCh37
NC_000011.8:g.36328297_36328355del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50826_-125-50768del MANE Select ENSP00000435050.1:n.-125-50826_-125-50768del
ENST00000527172.5:c.-291-43675_-291-43617del ENSP00000433708.1:n.-291-43675_-291-43617del
ENST00000529034.5:n.152-50826_152-50768del
ENST00000530639.5:c.-125-50826_-125-50768del ENSP00000435050.1:n.-125-50826_-125-50768del
ENST00000532121.5:c.-126+106_-126+164del ENSP00000433893.1:n.-126+106_-126+164del
NM_001160167.1:c.-125-50826_-125-50768del NP_001153639.1:n.-125-50826_-125-50768del
NM_001160167.2:c.-125-50826_-125-50768del MANE Select NP_001153639.1:n.-125-50826_-125-50768del
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