Canonical Allele Identifier: CA2613138597
Gene: PRR5L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350121A>G , CM000673.2:g.36350121A>G GRCh38
NC_000011.9:g.36371671A>G , CM000673.1:g.36371671A>G GRCh37
NC_000011.8:g.36328247A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50876A>G MANE Select ENSP00000435050.1:n.-125-50876A>G
ENST00000527172.5:c.-291-43725A>G ENSP00000433708.1:n.-291-43725A>G
ENST00000529034.5:n.152-50876A>G
ENST00000530639.5:c.-125-50876A>G ENSP00000435050.1:n.-125-50876A>G
ENST00000532121.5:c.-126+56A>G ENSP00000433893.1:n.-126+56A>G
NM_001160167.1:c.-125-50876A>G NP_001153639.1:n.-125-50876A>G
NM_001160167.2:c.-125-50876A>G MANE Select NP_001153639.1:n.-125-50876A>G