Canonical Allele Identifier: CA598574196
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1433359585
gnomAD v2: 11-36371753-AGTGTGTGTGGGGTGGGTGTGTGTGGGGGGTATAAGTGAGT-A
gnomAD v3: 11-36350203-AGTGTGTGTGGGGTGGGTGTGTGTGGGGGGTATAAGTGAGT-A
gnomAD v4: 11-36350203-AGTGTGTGTGGGGTGGGTGTGTGTGGGGGGTATAAGTGAGT-A
MyVariant Identifiers: chr11:g.36371754_36371793del (hg19) chr11:g.36350204_36350243del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350215_36350254del , CM000673.2:g.36350215_36350254del GRCh38
NC_000011.9:g.36371765_36371804del , CM000673.1:g.36371765_36371804del GRCh37
NC_000011.8:g.36328341_36328380del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50782_-125-50743del MANE Select ENSP00000435050.1:n.-125-50782_-125-50743...
ENST00000527172.5:c.-291-43631_-291-43592del ENSP00000433708.1:n.-291-43631_-291-43592...
ENST00000529034.5:n.152-50782_152-50743del
ENST00000530639.5:c.-125-50782_-125-50743del ENSP00000435050.1:n.-125-50782_-125-50743...
ENST00000532121.5:c.-126+150_-126+189del ENSP00000433893.1:n.-126+150_-126+189del
NM_001160167.1:c.-125-50782_-125-50743del NP_001153639.1:n.-125-50782_-125-50743del...
NM_001160167.2:c.-125-50782_-125-50743del MANE Select NP_001153639.1:n.-125-50782_-125-50743del...
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