Canonical Allele Identifier: CA936880966

Gene: PRR5L

Linked Data

• dbSNP Id: rs1856910547
• gnomAD v3: 11-36350053-T-C
• gnomAD v4: 11-36350053-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36350053T>C , CM000673.2:g.36350053T>C	GRCh38
NC_000011.9:g.36371603T>C , CM000673.1:g.36371603T>C	GRCh37
NC_000011.8:g.36328179T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000530639.6:c.-125-50944T>C MANE Select	ENSP00000435050.1:n.-125-50944T>C
ENST00000527172.5:c.-291-43793T>C	ENSP00000433708.1:n.-291-43793T>C
ENST00000529034.5:n.152-50944T>C
ENST00000530639.5:c.-125-50944T>C	ENSP00000435050.1:n.-125-50944T>C
ENST00000532121.5:c.-138T>C	ENSP00000433893.1:n.-138T>C
NM_001160167.1:c.-125-50944T>C	NP_001153639.1:n.-125-50944T>C
NM_001160167.2:c.-125-50944T>C MANE Select	NP_001153639.1:n.-125-50944T>C