Canonical Allele Identifier: CA675995384
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1401882697

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350216_36350230del , CM000673.2:g.36350216_36350230del GRCh38
NC_000011.9:g.36371766_36371780del , CM000673.1:g.36371766_36371780del GRCh37
NC_000011.8:g.36328342_36328356del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50781_-125-50767del MANE Select ENSP00000435050.1:n.-125-50781_-125-50767...
ENST00000527172.5:c.-291-43630_-291-43616del ENSP00000433708.1:n.-291-43630_-291-43616...
ENST00000529034.5:n.152-50781_152-50767del
ENST00000530639.5:c.-125-50781_-125-50767del ENSP00000435050.1:n.-125-50781_-125-50767...
ENST00000532121.5:c.-126+151_-126+165del ENSP00000433893.1:n.-126+151_-126+165del
NM_001160167.1:c.-125-50781_-125-50767del NP_001153639.1:n.-125-50781_-125-50767del...
NM_001160167.2:c.-125-50781_-125-50767del MANE Select NP_001153639.1:n.-125-50781_-125-50767del...