Canonical Allele Identifier: CA936881020
Gene: PRR5L HGNC NCBI

Linked Data

gnomAD v3: 11-36350167-AGGG-A
gnomAD v4: 11-36350167-AGGG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350168_36350170del , CM000673.2:g.36350168_36350170del GRCh38
NC_000011.9:g.36371718_36371720del , CM000673.1:g.36371718_36371720del GRCh37
NC_000011.8:g.36328294_36328296del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50829_-125-50827del MANE Select ENSP00000435050.1:n.-125-50829_-125-50827del
ENST00000527172.5:c.-291-43678_-291-43676del ENSP00000433708.1:n.-291-43678_-291-43676del
ENST00000529034.5:n.152-50829_152-50827del
ENST00000530639.5:c.-125-50829_-125-50827del ENSP00000435050.1:n.-125-50829_-125-50827del
ENST00000532121.5:c.-126+103_-126+105del ENSP00000433893.1:n.-126+103_-126+105del
NM_001160167.1:c.-125-50829_-125-50827del NP_001153639.1:n.-125-50829_-125-50827del
NM_001160167.2:c.-125-50829_-125-50827del MANE Select NP_001153639.1:n.-125-50829_-125-50827del
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