Linked Data
ClinVar Variation Id:
2160939
ClinVar RCV Id:
RCV003076211
dbSNP Id:
rs1990245659
gnomAD v4:
17-8288879-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8288879G>A , CM000679.2:g.8288879G>A | GRCh38 |
| NC_000017.10:g.8192197G>A , CM000679.1:g.8192197G>A | GRCh37 |
| NC_000017.9:g.8132922G>A | NCBI36 |
| NG_028189.1:g.5229G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226105.11:c.77+14G>A (RANGRF) MANE Select | ENSP00000226105.6:n.77+14G>A | |
| ENST00000226105.10:c.77+14G>A (RANGRF) | ENSP00000226105.6:n.77+14G>A | |
| ENST00000380067.6:c.*737C>T (SLC25A35) | ENSP00000369407.2:n.*737C>T | |
| ENST00000407006.8:c.77+14G>A (RANGRF) | ENSP00000383940.4:n.77+14G>A | |
| ENST00000439238.3:c.77+14G>A (RANGRF) | ENSP00000413190.3:n.77+14G>A | |
| ENST00000578849.1:n.167+14G>A (RANGRF) | ||
| ENST00000579192.5:c.*43-447C>T (SLC25A35) | ENSP00000462395.1:n.*43-447C>T | |
| ENST00000580340.5:c.*604C>T (SLC25A35) | ENSP00000464071.1:n.*604C>T | |
| ENST00000580434.5:c.77+14G>A (RANGRF) | ENSP00000462310.1:n.77+14G>A | |
| ENST00000581320.1:n.90+67C>T (SLC25A35) | ||
| ENST00000585311.5:c.*649C>T (SLC25A35) | ENSP00000464191.1:n.*649C>T | |
| NM_001177801.1:c.77+14G>A (RANGRF) | NP_001171272.1:n.77+14G>A | |
| NM_001177802.1:c.77+14G>A (RANGRF) | NP_001171273.1:n.77+14G>A | |
| NM_016492.4:c.77+14G>A (RANGRF) | NP_057576.2:n.77+14G>A | |
| NM_201520.1:c.*737C>T (SLC25A35) | NP_958928.1:n.*737C>T | |
| XM_005256618.3:c.77+14G>A (RANGRF) | XP_005256675.1:n.77+14G>A | |
| NM_001320871.1:c.*43-447C>T (SLC25A35) | NP_001307800.1:n.*43-447C>T | |
| NM_001320872.1:c.*604C>T (SLC25A35) | NP_001307801.1:n.*604C>T | |
| NM_001330127.1:c.77+14G>A (RANGRF) | NP_001317056.1:n.77+14G>A | |
| NM_201520.2:c.*737C>T (SLC25A35) | NP_958928.1:n.*737C>T | |
| NR_135484.1:n.2061C>T (SLC25A35) | ||
| NM_016492.5:c.77+14G>A (RANGRF) MANE Select | NP_057576.2:n.77+14G>A | |
| NM_001177801.2:c.77+14G>A (RANGRF) | NP_001171272.1:n.77+14G>A | |
| NM_001177802.2:c.77+14G>A (RANGRF) | NP_001171273.1:n.77+14G>A | |
| NM_001320871.2:c.*43-447C>T (SLC25A35) | NP_001307800.1:n.*43-447C>T | |
| NM_001330127.2:c.77+14G>A (RANGRF) | NP_001317056.1:n.77+14G>A | |
| NM_201520.3:c.*737C>T (SLC25A35) | NP_958928.1:n.*737C>T | |
| NR_135483.2:n.2282C>T (SLC25A35) | ||
| NM_001320872.2:c.*604C>T (SLC25A35) | NP_001307801.1:n.*604C>T | |
| NR_135484.2:n.2118C>T (SLC25A35) |