Canonical Allele Identifier: CA675995400
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1240155643
gnomAD v4: 11-36350215-G-A
MyVariant Identifiers: chr11:g.36371765G>A (hg19) chr11:g.36350215G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350215G>A , CM000673.2:g.36350215G>A GRCh38
NC_000011.9:g.36371765G>A , CM000673.1:g.36371765G>A GRCh37
NC_000011.8:g.36328341G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000530639.6:c.-125-50782G>A MANE Select ENSP00000435050.1:n.-125-50782G>A
ENST00000527172.5:c.-291-43631G>A ENSP00000433708.1:n.-291-43631G>A
ENST00000529034.5:n.152-50782G>A
ENST00000530639.5:c.-125-50782G>A ENSP00000435050.1:n.-125-50782G>A
ENST00000532121.5:c.-126+150G>A ENSP00000433893.1:n.-126+150G>A
NM_001160167.1:c.-125-50782G>A NP_001153639.1:n.-125-50782G>A
NM_001160167.2:c.-125-50782G>A MANE Select NP_001153639.1:n.-125-50782G>A
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