Linked Data
ClinVar Variation Id:
659442
dbSNP Id:
rs368516826
gnomAD v2:
7-117199695-T-C
gnomAD v3:
7-117559641-T-C
gnomAD v4:
7-117559641-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117559641T>C , CM000669.2:g.117559641T>C | GRCh38 |
| NC_000007.13:g.117199695T>C , CM000669.1:g.117199695T>C | GRCh37 |
| NC_000007.12:g.116986931T>C | NCBI36 |
| NG_016465.4:g.98858T>C , LRG_663:g.98858T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.1570T>C (CFTR) | ENSP00000497673.2:p.Cys524Arg | |
| ENST00000647978.2:c.*1284T>C (CFTR) | ENSP00000497658.1:n.*1284T>C | |
| ENST00000649781.2:c.1387T>C (CFTR) | ENSP00000497203.1:p.Cys463Arg | |
| ENST00000685018.2:c.1570T>C (CFTR) | ENSP00000510194.2:p.Cys524Arg | |
| ENST00000687278.2:c.1570T>C (CFTR) | ENSP00000509593.2:p.Cys524Arg | |
| ENST00000699585.1:c.1570T>C (CFTR) | ENSP00000514456.1:p.Cys524Arg | |
| ENST00000699596.1:c.1570T>C (CFTR) | ENSP00000514465.1:p.Cys524Arg | |
| ENST00000699597.1:c.*128T>C (CFTR) | ENSP00000514466.1:n.*128T>C | |
| ENST00000699598.1:c.1570T>C (CFTR) | ENSP00000514467.1:p.Cys524Arg | |
| ENST00000699599.1:c.1570T>C (CFTR) | ENSP00000514468.1:p.Cys524Arg | |
| ENST00000699600.1:c.1570T>C (CFTR) | ENSP00000514469.1:p.Cys524Arg | |
| ENST00000699601.1:c.1570T>C (CFTR) | ENSP00000514470.1:p.Cys524Arg | |
| ENST00000699602.1:c.1570T>C (CFTR) | ENSP00000514471.1:p.Cys524Arg | |
| ENST00000699604.1:c.*1394T>C (CFTR) | ENSP00000514472.1:n.*1394T>C | |
| ENST00000699605.1:c.1144T>C (CFTR) | ENSP00000514473.1:p.Cys382Arg | |
| ENST00000003084.11:c.1570T>C (CFTR) MANE Select | ENSP00000003084.6:p.Cys524Arg | |
| ENST00000647978.1:c.*1284T>C (CFTR) | ENSP00000497658.1:n.*1284T>C | |
| ENST00000648260.1:c.1387T>C (CFTR) | ENSP00000497957.1:p.Cys463Arg | |
| ENST00000649406.1:c.1387T>C (CFTR) | ENSP00000497965.1:p.Cys463Arg | |
| ENST00000649781.1:c.1387T>C (CFTR) | ENSP00000497203.1:p.Cys463Arg | |
| ENST00000003084.10:c.1570T>C (CFTR) | ENSP00000003084.6:p.Cys524Arg | |
| ENST00000426809.5:c.1480T>C (CFTR) | ENSP00000389119.1:p.Cys494Arg | |
| ENST00000472848.1:n.4T>C (CFTR) | ||
| NM_000492.3:c.1570T>C , LRG_663t1:c.1570T>C (CFTR) | NP_000483.3:p.Cys524Arg | |
| XM_011515751.1:c.1660T>C (CFTR) | XP_011514053.1:p.Cys554Arg | |
| XM_011515752.1:c.1660T>C (CFTR) | XP_011514054.1:p.Cys554Arg | |
| XM_011515753.1:c.1327T>C (CFTR) | XP_011514055.1:p.Cys443Arg | |
| XM_011515754.1:c.1327T>C (CFTR) | XP_011514056.1:p.Cys443Arg | |
| NR_149084.1:n.221+1092A>G (CFTR-AS1) | ||
| NM_000492.4:c.1570T>C (CFTR) MANE Select | NP_000483.3:p.Cys524Arg |