Canonical Allele Identifier: CA2613138539
Gene: PRR5L HGNC NCBI

Linked Data

gnomAD v4: 11-36350013-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350013C>A , CM000673.2:g.36350013C>A GRCh38
NC_000011.9:g.36371563C>A , CM000673.1:g.36371563C>A GRCh37
NC_000011.8:g.36328139C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50984C>A MANE Select ENSP00000435050.1:n.-125-50984C>A
ENST00000527172.5:c.-291-43833C>A ENSP00000433708.1:n.-291-43833C>A
ENST00000529034.5:n.152-50984C>A
ENST00000530639.5:c.-125-50984C>A ENSP00000435050.1:n.-125-50984C>A
ENST00000532121.5:c.-178C>A ENSP00000433893.1:n.-178C>A
NM_001160167.1:c.-125-50984C>A NP_001153639.1:n.-125-50984C>A
NM_001160167.2:c.-125-50984C>A MANE Select NP_001153639.1:n.-125-50984C>A
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