Canonical Allele Identifier: CA675995303
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1340873105
MyVariant Identifiers: chr11:g.36371567A>T (hg19) chr11:g.36350017A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350017A>T , CM000673.2:g.36350017A>T GRCh38
NC_000011.9:g.36371567A>T , CM000673.1:g.36371567A>T GRCh37
NC_000011.8:g.36328143A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50980A>T MANE Select ENSP00000435050.1:n.-125-50980A>T
ENST00000527172.5:c.-291-43829A>T ENSP00000433708.1:n.-291-43829A>T
ENST00000529034.5:n.152-50980A>T
ENST00000530639.5:c.-125-50980A>T ENSP00000435050.1:n.-125-50980A>T
ENST00000532121.5:c.-174A>T ENSP00000433893.1:n.-174A>T
NM_001160167.1:c.-125-50980A>T NP_001153639.1:n.-125-50980A>T
NM_001160167.2:c.-125-50980A>T MANE Select NP_001153639.1:n.-125-50980A>T
Search 100 bp 5'
Search 100 bp 3'