Canonical Allele Identifier: CA1964082242
Gene: PRR5L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350117A= , CM000673.2:g.36350117A= GRCh38
NC_000011.9:g.36371667A= , CM000673.1:g.36371667A= GRCh37
NC_000011.8:g.36328243A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50880A= MANE Select ENSP00000435050.1:n.-125-50880A=
ENST00000527172.5:c.-291-43729A= ENSP00000433708.1:n.-291-43729A=
ENST00000529034.5:n.152-50880A=
ENST00000530639.5:c.-125-50880A= ENSP00000435050.1:n.-125-50880A=
ENST00000532121.5:c.-126+52A= ENSP00000433893.1:n.-126+52A=
NM_001160167.1:c.-125-50880A= NP_001153639.1:n.-125-50880A=
NM_001160167.2:c.-125-50880A= MANE Select NP_001153639.1:n.-125-50880A=