Canonical Allele Identifier: CA1964082235
Gene: PRR5L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350116G= , CM000673.2:g.36350116G= GRCh38
NC_000011.9:g.36371666G= , CM000673.1:g.36371666G= GRCh37
NC_000011.8:g.36328242G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50881G= MANE Select ENSP00000435050.1:n.-125-50881G=
ENST00000527172.5:c.-291-43730G= ENSP00000433708.1:n.-291-43730G=
ENST00000529034.5:n.152-50881G=
ENST00000530639.5:c.-125-50881G= ENSP00000435050.1:n.-125-50881G=
ENST00000532121.5:c.-126+51G= ENSP00000433893.1:n.-126+51G=
NM_001160167.1:c.-125-50881G= NP_001153639.1:n.-125-50881G=
NM_001160167.2:c.-125-50881G= MANE Select NP_001153639.1:n.-125-50881G=