Canonical Allele Identifier: CA936881019
Gene: PRR5L HGNC NCBI

Linked Data

gnomAD v3: 11-36350167-AGGGTGGGTGTGTGTGTGGGAGGGT-A
gnomAD v4: 11-36350167-AGGGTGGGTGTGTGTGTGGGAGGGT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350179_36350202del , CM000673.2:g.36350179_36350202del GRCh38
NC_000011.9:g.36371729_36371752del , CM000673.1:g.36371729_36371752del GRCh37
NC_000011.8:g.36328305_36328328del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50818_-125-50795del MANE Select ENSP00000435050.1:n.-125-50818_-125-50795del
ENST00000527172.5:c.-291-43667_-291-43644del ENSP00000433708.1:n.-291-43667_-291-43644del
ENST00000529034.5:n.152-50818_152-50795del
ENST00000530639.5:c.-125-50818_-125-50795del ENSP00000435050.1:n.-125-50818_-125-50795del
ENST00000532121.5:c.-126+114_-126+137del ENSP00000433893.1:n.-126+114_-126+137del
NM_001160167.1:c.-125-50818_-125-50795del NP_001153639.1:n.-125-50818_-125-50795del
NM_001160167.2:c.-125-50818_-125-50795del MANE Select NP_001153639.1:n.-125-50818_-125-50795del
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