Linked Data
ClinVar Variation Id:
2203021
ClinVar RCV Id:
RCV002634360
dbSNP Id:
rs1323030006
gnomAD v2:
1-93303051-A-G
gnomAD v4:
1-92837494-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.92837494A>G , CM000663.2:g.92837494A>G | GRCh38 |
| NC_000001.10:g.93303051A>G , CM000663.1:g.93303051A>G | GRCh37 |
| NC_000001.9:g.93075639A>G | NCBI36 |
| NG_011779.1:g.10458A>G | |
| NG_033051.1:g.129029T>C | |
| NG_011779.2:g.10509A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370321.8:c.566A>G (RPL5) MANE Select | ENSP00000359345.2:p.Glu189Gly | |
| ENST00000645119.1:c.324+2581A>G (RPL5) | ENSP00000493811.1:n.324+2581A>G | |
| ENST00000645300.1:c.416A>G (RPL5) | ENSP00000495589.1:p.Glu139Gly | |
| ENST00000645908.1:n.300A>G (RPL5) | ||
| ENST00000370321.7:c.566A>G (RPL5) | ENSP00000359345.2:p.Glu189Gly | |
| ENST00000497519.1:n.885A>G (RPL5) | ||
| ENST00000615519.4:c.475-4460T>C (DIPK1A) | ENSP00000483279.1:n.475-4460T>C | |
| NM_000969.3:c.566A>G (RPL5) | NP_000960.2:p.Glu189Gly | |
| NM_001252273.1:c.475-4460T>C (DIPK1A) | NP_001239202.1:n.475-4460T>C | |
| NM_000969.5:c.566A>G (RPL5) MANE Select | NP_000960.2:p.Glu189Gly | |
| NR_146333.1:n.625A>G (RPL5) | ||
| NM_001252273.2:c.475-4460T>C (DIPK1A) | NP_001239202.1:n.475-4460T>C |