Canonical Allele Identifier: CA675995358
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1162375794
gnomAD v3: 11-36350157-GGTGTGTGGGAGGGTGGGTGT-G
gnomAD v4: 11-36350157-GGTGTGTGGGAGGGTGGGTGT-G
MyVariant Identifiers: chr11:g.36371708_36371727del (hg19) chr11:g.36350158_36350177del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350177_36350196del , CM000673.2:g.36350177_36350196del GRCh38
NC_000011.9:g.36371727_36371746del , CM000673.1:g.36371727_36371746del GRCh37
NC_000011.8:g.36328303_36328322del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50820_-125-50801del MANE Select ENSP00000435050.1:n.-125-50820_-125-50801del
ENST00000527172.5:c.-291-43669_-291-43650del ENSP00000433708.1:n.-291-43669_-291-43650del
ENST00000529034.5:n.152-50820_152-50801del
ENST00000530639.5:c.-125-50820_-125-50801del ENSP00000435050.1:n.-125-50820_-125-50801del
ENST00000532121.5:c.-126+112_-126+131del ENSP00000433893.1:n.-126+112_-126+131del
NM_001160167.1:c.-125-50820_-125-50801del NP_001153639.1:n.-125-50820_-125-50801del
NM_001160167.2:c.-125-50820_-125-50801del MANE Select NP_001153639.1:n.-125-50820_-125-50801del
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