Canonical Allele Identifier: CA598574186
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1287506669

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350145_36350156del , CM000673.2:g.36350145_36350156del GRCh38
NC_000011.9:g.36371695_36371706del , CM000673.1:g.36371695_36371706del GRCh37
NC_000011.8:g.36328271_36328282del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50852_-125-50841del MANE Select ENSP00000435050.1:n.-125-50852_-125-50841...
ENST00000527172.5:c.-291-43701_-291-43690del ENSP00000433708.1:n.-291-43701_-291-43690...
ENST00000529034.5:n.152-50852_152-50841del
ENST00000530639.5:c.-125-50852_-125-50841del ENSP00000435050.1:n.-125-50852_-125-50841...
ENST00000532121.5:c.-126+80_-126+91del ENSP00000433893.1:n.-126+80_-126+91del
NM_001160167.1:c.-125-50852_-125-50841del NP_001153639.1:n.-125-50852_-125-50841del...
NM_001160167.2:c.-125-50852_-125-50841del MANE Select NP_001153639.1:n.-125-50852_-125-50841del...