Canonical Allele Identifier: CA2791060494
Gene: PRR5L HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350211_36350233del , CM000673.2:g.36350211_36350233del GRCh38
NC_000011.9:g.36371761_36371783del , CM000673.1:g.36371761_36371783del GRCh37
NC_000011.8:g.36328337_36328359del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50786_-125-50764del MANE Select ENSP00000435050.1:n.-125-50786_-125-50764del
ENST00000527172.5:c.-291-43635_-291-43613del ENSP00000433708.1:n.-291-43635_-291-43613del
ENST00000529034.5:n.152-50786_152-50764del
ENST00000530639.5:c.-125-50786_-125-50764del ENSP00000435050.1:n.-125-50786_-125-50764del
ENST00000532121.5:c.-126+146_-126+168del ENSP00000433893.1:n.-126+146_-126+168del
NM_001160167.1:c.-125-50786_-125-50764del NP_001153639.1:n.-125-50786_-125-50764del
NM_001160167.2:c.-125-50786_-125-50764del MANE Select NP_001153639.1:n.-125-50786_-125-50764del
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