Canonical Allele Identifier: CA1964082105
Gene: PRR5L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350035G= , CM000673.2:g.36350035G= GRCh38
NC_000011.9:g.36371585G= , CM000673.1:g.36371585G= GRCh37
NC_000011.8:g.36328161G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50962G= MANE Select ENSP00000435050.1:n.-125-50962G=
ENST00000527172.5:c.-291-43811G= ENSP00000433708.1:n.-291-43811G=
ENST00000529034.5:n.152-50962G=
ENST00000530639.5:c.-125-50962G= ENSP00000435050.1:n.-125-50962G=
ENST00000532121.5:c.-156G= ENSP00000433893.1:n.-156G=
NM_001160167.1:c.-125-50962G= NP_001153639.1:n.-125-50962G=
NM_001160167.2:c.-125-50962G= MANE Select NP_001153639.1:n.-125-50962G=