Canonical Allele Identifier: CA2613138549

Gene: PRR5L

Linked Data

• gnomAD v4: 11-36350031-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36350031T>C , CM000673.2:g.36350031T>C	GRCh38
NC_000011.9:g.36371581T>C , CM000673.1:g.36371581T>C	GRCh37
NC_000011.8:g.36328157T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530639.6:c.-125-50966T>C MANE Select	ENSP00000435050.1:n.-125-50966T>C
ENST00000527172.5:c.-291-43815T>C	ENSP00000433708.1:n.-291-43815T>C
ENST00000529034.5:n.152-50966T>C
ENST00000530639.5:c.-125-50966T>C	ENSP00000435050.1:n.-125-50966T>C
ENST00000532121.5:c.-160T>C	ENSP00000433893.1:n.-160T>C
NM_001160167.1:c.-125-50966T>C	NP_001153639.1:n.-125-50966T>C
NM_001160167.2:c.-125-50966T>C MANE Select	NP_001153639.1:n.-125-50966T>C