Linked Data
ClinVar Variation Id:
1539434
ClinVar RCV Id:
RCV002162498
dbSNP Id:
rs755018574
ExAC:
17:8192281 C / A
gnomAD v2:
17-8192281-C-A
gnomAD v4:
17-8288963-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8288963C>A , CM000679.2:g.8288963C>A | GRCh38 |
| NC_000017.10:g.8192281C>A , CM000679.1:g.8192281C>A | GRCh37 |
| NC_000017.9:g.8133006C>A | NCBI36 |
| NG_028189.1:g.5313C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226105.11:c.85C>A (RANGRF) MANE Select | ENSP00000226105.6:p.Arg29= | |
| ENST00000226105.10:c.85C>A (RANGRF) | ENSP00000226105.6:p.Arg29= | |
| ENST00000380067.6:c.*653G>T (SLC25A35) | ENSP00000369407.2:n.*653G>T | |
| ENST00000407006.8:c.85C>A (RANGRF) | ENSP00000383940.4:p.Arg29= | |
| ENST00000439238.3:c.85C>A (RANGRF) | ENSP00000413190.3:p.Arg29= | |
| ENST00000578849.1:n.175C>A (RANGRF) | ||
| ENST00000579192.5:c.*43-531G>T (SLC25A35) | ENSP00000462395.1:n.*43-531G>T | |
| ENST00000580340.5:c.*520G>T (SLC25A35) | ENSP00000464071.1:n.*520G>T | |
| ENST00000580434.5:c.85C>A (RANGRF) | ENSP00000462310.1:p.Arg29= | |
| ENST00000580777.1:n.79C>A (RANGRF) | ||
| ENST00000581320.1:n.73G>T (SLC25A35) | ||
| ENST00000585311.5:c.*565G>T (SLC25A35) | ENSP00000464191.1:n.*565G>T | |
| NM_001177801.1:c.85C>A (RANGRF) | NP_001171272.1:p.Arg29= | |
| NM_001177802.1:c.85C>A (RANGRF) | NP_001171273.1:p.Arg29= | |
| NM_016492.4:c.85C>A (RANGRF) | NP_057576.2:p.Arg29= | |
| NM_201520.1:c.*653G>T (SLC25A35) | NP_958928.1:n.*653G>T | |
| XM_005256618.3:c.85C>A (RANGRF) | XP_005256675.1:p.Arg29= | |
| NM_001320871.1:c.*43-531G>T (SLC25A35) | NP_001307800.1:n.*43-531G>T | |
| NM_001320872.1:c.*520G>T (SLC25A35) | NP_001307801.1:n.*520G>T | |
| NM_001330127.1:c.85C>A (RANGRF) | NP_001317056.1:p.Arg29= | |
| NM_201520.2:c.*653G>T (SLC25A35) | NP_958928.1:n.*653G>T | |
| NR_135484.1:n.1977G>T (SLC25A35) | ||
| NM_016492.5:c.85C>A (RANGRF) MANE Select | NP_057576.2:p.Arg29= | |
| NM_001177801.2:c.85C>A (RANGRF) | NP_001171272.1:p.Arg29= | |
| NM_001177802.2:c.85C>A (RANGRF) | NP_001171273.1:p.Arg29= | |
| NM_001320871.2:c.*43-531G>T (SLC25A35) | NP_001307800.1:n.*43-531G>T | |
| NM_001330127.2:c.85C>A (RANGRF) | NP_001317056.1:p.Arg29= | |
| NM_201520.3:c.*653G>T (SLC25A35) | NP_958928.1:n.*653G>T | |
| NR_135483.2:n.2198G>T (SLC25A35) | ||
| NM_001320872.2:c.*520G>T (SLC25A35) | NP_001307801.1:n.*520G>T | |
| NR_135484.2:n.2034G>T (SLC25A35) |