Linked Data
dbSNP Id:
rs369811492
ExAC:
1:93302984 A / G
gnomAD v2:
1-93302984-A-G
gnomAD v3:
1-92837427-A-G
gnomAD v4:
1-92837427-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.92837427A>G , CM000663.2:g.92837427A>G | GRCh38 |
| NC_000001.10:g.93302984A>G , CM000663.1:g.93302984A>G | GRCh37 |
| NC_000001.9:g.93075572A>G | NCBI36 |
| NG_011779.1:g.10391A>G | |
| NG_033051.1:g.129096T>C | |
| NG_011779.2:g.10442A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370321.8:c.528-29A>G (RPL5) MANE Select | ENSP00000359345.2:n.528-29A>G | |
| ENST00000645119.1:c.324+2514A>G (RPL5) | ENSP00000493811.1:n.324+2514A>G | |
| ENST00000645300.1:c.378-29A>G (RPL5) | ENSP00000495589.1:n.378-29A>G | |
| ENST00000645908.1:n.262-29A>G (RPL5) | ||
| ENST00000315741.5:c.378-29A>G (RPL5) | ENSP00000359338.2:n.378-29A>G | |
| ENST00000370321.7:c.528-29A>G (RPL5) | ENSP00000359345.2:n.528-29A>G | |
| ENST00000497519.1:n.818A>G (RPL5) | ||
| ENST00000615519.4:c.475-4393T>C (DIPK1A) | ENSP00000483279.1:n.475-4393T>C | |
| NM_000969.3:c.528-29A>G (RPL5) | NP_000960.2:n.528-29A>G | |
| NM_001252273.1:c.475-4393T>C (DIPK1A) | NP_001239202.1:n.475-4393T>C | |
| NM_000969.5:c.528-29A>G (RPL5) MANE Select | NP_000960.2:n.528-29A>G | |
| NR_146333.1:n.587-29A>G (RPL5) | ||
| NM_001252273.2:c.475-4393T>C (DIPK1A) | NP_001239202.1:n.475-4393T>C |