Canonical Allele Identifier: CA936881003
Gene: PRR5L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350167_36350229del , CM000673.2:g.36350167_36350229del GRCh38
NC_000011.9:g.36371717_36371779del , CM000673.1:g.36371717_36371779del GRCh37
NC_000011.8:g.36328293_36328355del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50830_-125-50768del MANE Select ENSP00000435050.1:n.-125-50830_-125-50768del
ENST00000527172.5:c.-291-43679_-291-43617del ENSP00000433708.1:n.-291-43679_-291-43617del
ENST00000529034.5:n.152-50830_152-50768del
ENST00000530639.5:c.-125-50830_-125-50768del ENSP00000435050.1:n.-125-50830_-125-50768del
ENST00000532121.5:c.-126+102_-126+164del ENSP00000433893.1:n.-126+102_-126+164del
NM_001160167.1:c.-125-50830_-125-50768del NP_001153639.1:n.-125-50830_-125-50768del
NM_001160167.2:c.-125-50830_-125-50768del MANE Select NP_001153639.1:n.-125-50830_-125-50768del