Canonical Allele Identifier: CA220699104

Gene: PRR5L

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36350207T>C , CM000673.2:g.36350207T>C	GRCh38
NC_000011.9:g.36371757T>C , CM000673.1:g.36371757T>C	GRCh37
NC_000011.8:g.36328333T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530639.6:c.-125-50790T>C MANE Select	ENSP00000435050.1:n.-125-50790T>C
ENST00000527172.5:c.-291-43639T>C	ENSP00000433708.1:n.-291-43639T>C
ENST00000529034.5:n.152-50790T>C
ENST00000530639.5:c.-125-50790T>C	ENSP00000435050.1:n.-125-50790T>C
ENST00000532121.5:c.-126+142T>C	ENSP00000433893.1:n.-126+142T>C
NM_001160167.1:c.-125-50790T>C	NP_001153639.1:n.-125-50790T>C
NM_001160167.2:c.-125-50790T>C MANE Select	NP_001153639.1:n.-125-50790T>C