Canonical Allele Identifier: CA2613138640
Gene: PRR5L HGNC NCBI

Linked Data

gnomAD v4: 11-36350161-TGTGGGAGGGTGGGTGTGTGTGTGGGAGG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350167_36350194del , CM000673.2:g.36350167_36350194del GRCh38
NC_000011.9:g.36371717_36371744del , CM000673.1:g.36371717_36371744del GRCh37
NC_000011.8:g.36328293_36328320del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50830_-125-50803del MANE Select ENSP00000435050.1:n.-125-50830_-125-50803del
ENST00000527172.5:c.-291-43679_-291-43652del ENSP00000433708.1:n.-291-43679_-291-43652del
ENST00000529034.5:n.152-50830_152-50803del
ENST00000530639.5:c.-125-50830_-125-50803del ENSP00000435050.1:n.-125-50830_-125-50803del
ENST00000532121.5:c.-126+102_-126+129del ENSP00000433893.1:n.-126+102_-126+129del
NM_001160167.1:c.-125-50830_-125-50803del NP_001153639.1:n.-125-50830_-125-50803del
NM_001160167.2:c.-125-50830_-125-50803del MANE Select NP_001153639.1:n.-125-50830_-125-50803del
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