Canonical Allele Identifier: CA1964082249
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1856911377

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350123G>A , CM000673.2:g.36350123G>A GRCh38
NC_000011.9:g.36371673G>A , CM000673.1:g.36371673G>A GRCh37
NC_000011.8:g.36328249G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50874G>A MANE Select ENSP00000435050.1:n.-125-50874G>A
ENST00000527172.5:c.-291-43723G>A ENSP00000433708.1:n.-291-43723G>A
ENST00000529034.5:n.152-50874G>A
ENST00000530639.5:c.-125-50874G>A ENSP00000435050.1:n.-125-50874G>A
ENST00000532121.5:c.-126+58G>A ENSP00000433893.1:n.-126+58G>A
NM_001160167.1:c.-125-50874G>A NP_001153639.1:n.-125-50874G>A
NM_001160167.2:c.-125-50874G>A MANE Select NP_001153639.1:n.-125-50874G>A