Canonical Allele Identifier: CA675995304
Gene: PRR5L HGNC NCBI

Linked Data

dbSNP Id: rs1299873132

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36350035G>C , CM000673.2:g.36350035G>C GRCh38
NC_000011.9:g.36371585G>C , CM000673.1:g.36371585G>C GRCh37
NC_000011.8:g.36328161G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000530639.6:c.-125-50962G>C MANE Select ENSP00000435050.1:n.-125-50962G>C
ENST00000527172.5:c.-291-43811G>C ENSP00000433708.1:n.-291-43811G>C
ENST00000529034.5:n.152-50962G>C
ENST00000530639.5:c.-125-50962G>C ENSP00000435050.1:n.-125-50962G>C
ENST00000532121.5:c.-156G>C ENSP00000433893.1:n.-156G>C
NM_001160167.1:c.-125-50962G>C NP_001153639.1:n.-125-50962G>C
NM_001160167.2:c.-125-50962G>C MANE Select NP_001153639.1:n.-125-50962G>C