Linked Data
ClinVar Variation Id:
1772521
ClinVar RCV Id:
RCV002392083
dbSNP Id:
rs1799418198
MyVariant Identifiers:
chr7:g.117199556T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117559502T>C , CM000669.2:g.117559502T>C | GRCh38 |
| NC_000007.13:g.117199556T>C , CM000669.1:g.117199556T>C | GRCh37 |
| NC_000007.12:g.116986792T>C | NCBI36 |
| NG_016465.4:g.98719T>C , LRG_663:g.98719T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647720.2:c.1431T>C (CFTR) | ENSP00000497673.2:p.Pro477= | |
| ENST00000647978.2:c.*1145T>C (CFTR) | ENSP00000497658.1:n.*1145T>C | |
| ENST00000649781.2:c.1248T>C (CFTR) | ENSP00000497203.1:p.Pro416= | |
| ENST00000685018.2:c.1431T>C (CFTR) | ENSP00000510194.2:p.Pro477= | |
| ENST00000687278.2:c.1431T>C (CFTR) | ENSP00000509593.2:p.Pro477= | |
| ENST00000699585.1:c.1431T>C (CFTR) | ENSP00000514456.1:p.Pro477= | |
| ENST00000699596.1:c.1431T>C (CFTR) | ENSP00000514465.1:p.Pro477= | |
| ENST00000699597.1:c.1426T>C (CFTR) | ENSP00000514466.1:p.Phe476Leu | |
| ENST00000699598.1:c.1431T>C (CFTR) | ENSP00000514467.1:p.Pro477= | |
| ENST00000699599.1:c.1431T>C (CFTR) | ENSP00000514468.1:p.Pro477= | |
| ENST00000699600.1:c.1431T>C (CFTR) | ENSP00000514469.1:p.Pro477= | |
| ENST00000699601.1:c.1431T>C (CFTR) | ENSP00000514470.1:p.Pro477= | |
| ENST00000699602.1:c.1431T>C (CFTR) | ENSP00000514471.1:p.Pro477= | |
| ENST00000699604.1:c.*1255T>C (CFTR) | ENSP00000514472.1:n.*1255T>C | |
| ENST00000699605.1:c.1005T>C (CFTR) | ENSP00000514473.1:p.Pro335= | |
| ENST00000003084.11:c.1431T>C (CFTR) MANE Select | ENSP00000003084.6:p.Pro477= | |
| ENST00000647978.1:c.*1145T>C (CFTR) | ENSP00000497658.1:n.*1145T>C | |
| ENST00000648260.1:c.1248T>C (CFTR) | ENSP00000497957.1:p.Pro416= | |
| ENST00000649406.1:c.1248T>C (CFTR) | ENSP00000497965.1:p.Pro416= | |
| ENST00000649781.1:c.1248T>C (CFTR) | ENSP00000497203.1:p.Pro416= | |
| ENST00000003084.10:c.1431T>C (CFTR) | ENSP00000003084.6:p.Pro477= | |
| ENST00000426809.5:c.1341T>C (CFTR) | ENSP00000389119.1:p.Pro447= | |
| NM_000492.3:c.1431T>C , LRG_663t1:c.1431T>C (CFTR) | NP_000483.3:p.Pro477= | |
| XM_011515751.1:c.1521T>C (CFTR) | XP_011514053.1:p.Pro507= | |
| XM_011515752.1:c.1521T>C (CFTR) | XP_011514054.1:p.Pro507= | |
| XM_011515753.1:c.1188T>C (CFTR) | XP_011514055.1:p.Pro396= | |
| XM_011515754.1:c.1188T>C (CFTR) | XP_011514056.1:p.Pro396= | |
| NR_149084.1:n.221+1231A>G (CFTR-AS1) | ||
| NM_000492.4:c.1431T>C (CFTR) MANE Select | NP_000483.3:p.Pro477= |