Canonical Allele Identifier: CA936881000
Gene: PRR5L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350159_36350169del , CM000673.2:g.36350159_36350169del GRCh38
NC_000011.9:g.36371709_36371719del , CM000673.1:g.36371709_36371719del GRCh37
NC_000011.8:g.36328285_36328295del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50838_-125-50828del MANE Select ENSP00000435050.1:n.-125-50838_-125-50828del
ENST00000527172.5:c.-291-43687_-291-43677del ENSP00000433708.1:n.-291-43687_-291-43677del
ENST00000529034.5:n.152-50838_152-50828del
ENST00000530639.5:c.-125-50838_-125-50828del ENSP00000435050.1:n.-125-50838_-125-50828del
ENST00000532121.5:c.-126+94_-126+104del ENSP00000433893.1:n.-126+94_-126+104del
NM_001160167.1:c.-125-50838_-125-50828del NP_001153639.1:n.-125-50838_-125-50828del
NM_001160167.2:c.-125-50838_-125-50828del MANE Select NP_001153639.1:n.-125-50838_-125-50828del