Canonical Allele Identifier: CA598574185
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1402078911

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350059A>G , CM000673.2:g.36350059A>G GRCh38
NC_000011.9:g.36371609A>G , CM000673.1:g.36371609A>G GRCh37
NC_000011.8:g.36328185A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50938A>G MANE Select ENSP00000435050.1:n.-125-50938A>G
ENST00000527172.5:c.-291-43787A>G ENSP00000433708.1:n.-291-43787A>G
ENST00000529034.5:n.152-50938A>G
ENST00000530639.5:c.-125-50938A>G ENSP00000435050.1:n.-125-50938A>G
ENST00000532121.5:c.-132A>G ENSP00000433893.1:n.-132A>G
NM_001160167.1:c.-125-50938A>G NP_001153639.1:n.-125-50938A>G
NM_001160167.2:c.-125-50938A>G MANE Select NP_001153639.1:n.-125-50938A>G