Canonical Allele Identifier: CA220699083
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1037341024
gnomAD v2: 11-36371649-G-A
gnomAD v3: 11-36350099-G-A
gnomAD v4: 11-36350099-G-A
MyVariant Identifiers: chr11:g.36371649G>A (hg19) chr11:g.36350099G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350099G>A , CM000673.2:g.36350099G>A GRCh38
NC_000011.9:g.36371649G>A , CM000673.1:g.36371649G>A GRCh37
NC_000011.8:g.36328225G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50898G>A MANE Select ENSP00000435050.1:n.-125-50898G>A
ENST00000527172.5:c.-291-43747G>A ENSP00000433708.1:n.-291-43747G>A
ENST00000529034.5:n.152-50898G>A
ENST00000530639.5:c.-125-50898G>A ENSP00000435050.1:n.-125-50898G>A
ENST00000532121.5:c.-126+34G>A ENSP00000433893.1:n.-126+34G>A
NM_001160167.1:c.-125-50898G>A NP_001153639.1:n.-125-50898G>A
NM_001160167.2:c.-125-50898G>A MANE Select NP_001153639.1:n.-125-50898G>A
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