Canonical Allele Identifier: CA936881002
Gene: PRR5L HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350168_36350255del , CM000673.2:g.36350168_36350255del GRCh38
NC_000011.9:g.36371718_36371805del , CM000673.1:g.36371718_36371805del GRCh37
NC_000011.8:g.36328294_36328381del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50829_-125-50742del MANE Select ENSP00000435050.1:n.-125-50829_-125-50742...
ENST00000527172.5:c.-291-43678_-291-43591del ENSP00000433708.1:n.-291-43678_-291-43591...
ENST00000529034.5:n.152-50829_152-50742del
ENST00000530639.5:c.-125-50829_-125-50742del ENSP00000435050.1:n.-125-50829_-125-50742...
ENST00000532121.5:c.-126+103_-126+190del ENSP00000433893.1:n.-126+103_-126+190del
NM_001160167.1:c.-125-50829_-125-50742del NP_001153639.1:n.-125-50829_-125-50742del...
NM_001160167.2:c.-125-50829_-125-50742del MANE Select NP_001153639.1:n.-125-50829_-125-50742del...