Canonical Allele Identifier: CA1964082192
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1856910935
gnomAD v4: 11-36350089-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350089A>G , CM000673.2:g.36350089A>G GRCh38
NC_000011.9:g.36371639A>G , CM000673.1:g.36371639A>G GRCh37
NC_000011.8:g.36328215A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50908A>G MANE Select ENSP00000435050.1:n.-125-50908A>G
ENST00000527172.5:c.-291-43757A>G ENSP00000433708.1:n.-291-43757A>G
ENST00000529034.5:n.152-50908A>G
ENST00000530639.5:c.-125-50908A>G ENSP00000435050.1:n.-125-50908A>G
ENST00000532121.5:c.-126+24A>G ENSP00000433893.1:n.-126+24A>G
NM_001160167.1:c.-125-50908A>G NP_001153639.1:n.-125-50908A>G
NM_001160167.2:c.-125-50908A>G MANE Select NP_001153639.1:n.-125-50908A>G
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