Canonical Allele Identifier: CA524696714

Linked Data

dbSNP Id: rs1458899932
gnomAD v2: 1-93302989-A-G
gnomAD v4: 1-92837432-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837432A>G , CM000663.2:g.92837432A>G GRCh38
NC_000001.10:g.93302989A>G , CM000663.1:g.93302989A>G GRCh37
NC_000001.9:g.93075577A>G NCBI36
NG_011779.1:g.10396A>G
NG_033051.1:g.129091T>C
NG_011779.2:g.10447A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.528-24A>G (RPL5) MANE Select ENSP00000359345.2:n.528-24A>G
ENST00000645119.1:c.324+2519A>G (RPL5) ENSP00000493811.1:n.324+2519A>G
ENST00000645300.1:c.378-24A>G (RPL5) ENSP00000495589.1:n.378-24A>G
ENST00000645908.1:n.262-24A>G (RPL5)
ENST00000315741.5:c.378-24A>G (RPL5) ENSP00000359338.2:n.378-24A>G
ENST00000370321.7:c.528-24A>G (RPL5) ENSP00000359345.2:n.528-24A>G
ENST00000497519.1:n.823A>G (RPL5)
ENST00000615519.4:c.475-4398T>C (DIPK1A) ENSP00000483279.1:n.475-4398T>C
NM_000969.3:c.528-24A>G (RPL5) NP_000960.2:n.528-24A>G
NM_001252273.1:c.475-4398T>C (DIPK1A) NP_001239202.1:n.475-4398T>C
NM_000969.5:c.528-24A>G (RPL5) MANE Select NP_000960.2:n.528-24A>G
NR_146333.1:n.587-24A>G (RPL5)
NM_001252273.2:c.475-4398T>C (DIPK1A) NP_001239202.1:n.475-4398T>C