Linked Data
ClinVar Variation Id:
43576
ClinVar RCV Id:
RCV000036518
RCV000119037
RCV000231696
RCV000422767
RCV000844954
RCV001027903
RCV001588847
dbSNP Id:
rs1800095
ExAC:
7:117199709 G / A
gnomAD v2:
7-117199709-G-A
gnomAD v3:
7-117559655-G-A
gnomAD v4:
7-117559655-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117559655G>A , CM000669.2:g.117559655G>A | GRCh38 |
| NC_000007.13:g.117199709G>A , CM000669.1:g.117199709G>A | GRCh37 |
| NC_000007.12:g.116986945G>A | NCBI36 |
| NG_016465.4:g.98872G>A , LRG_663:g.98872G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.1584G>A (CFTR) | ENSP00000497673.2:p.Glu528= | |
| ENST00000647978.2:c.*1298G>A (CFTR) | ENSP00000497658.1:n.*1298G>A | |
| ENST00000649781.2:c.1401G>A (CFTR) | ENSP00000497203.1:p.Glu467= | |
| ENST00000685018.2:c.1584G>A (CFTR) | ENSP00000510194.2:p.Glu528= | |
| ENST00000687278.2:c.1584G>A (CFTR) | ENSP00000509593.2:p.Glu528= | |
| ENST00000699585.1:c.1584G>A (CFTR) | ENSP00000514456.1:p.Glu528= | |
| ENST00000699596.1:c.1584G>A (CFTR) | ENSP00000514465.1:p.Glu528= | |
| ENST00000699597.1:c.*142G>A (CFTR) | ENSP00000514466.1:n.*142G>A | |
| ENST00000699598.1:c.1584G>A (CFTR) | ENSP00000514467.1:p.Glu528= | |
| ENST00000699599.1:c.1584G>A (CFTR) | ENSP00000514468.1:p.Glu528= | |
| ENST00000699600.1:c.1584G>A (CFTR) | ENSP00000514469.1:p.Glu528= | |
| ENST00000699601.1:c.1584G>A (CFTR) | ENSP00000514470.1:p.Glu528= | |
| ENST00000699602.1:c.1584G>A (CFTR) | ENSP00000514471.1:p.Glu528= | |
| ENST00000699604.1:c.*1408G>A (CFTR) | ENSP00000514472.1:n.*1408G>A | |
| ENST00000699605.1:c.1158G>A (CFTR) | ENSP00000514473.1:p.Glu386= | |
| ENST00000003084.11:c.1584G>A (CFTR) MANE Select | ENSP00000003084.6:p.Glu528= | |
| ENST00000647978.1:c.*1298G>A (CFTR) | ENSP00000497658.1:n.*1298G>A | |
| ENST00000648260.1:c.1401G>A (CFTR) | ENSP00000497957.1:p.Glu467= | |
| ENST00000649406.1:c.1401G>A (CFTR) | ENSP00000497965.1:p.Glu467= | |
| ENST00000649781.1:c.1401G>A (CFTR) | ENSP00000497203.1:p.Glu467= | |
| ENST00000003084.10:c.1584G>A (CFTR) | ENSP00000003084.6:p.Glu528= | |
| ENST00000426809.5:c.1494G>A (CFTR) | ENSP00000389119.1:p.Glu498= | |
| ENST00000472848.1:n.18G>A (CFTR) | ||
| NM_000492.3:c.1584G>A , LRG_663t1:c.1584G>A (CFTR) | NP_000483.3:p.Glu528= | |
| XM_011515751.1:c.1674G>A (CFTR) | XP_011514053.1:p.Glu558= | |
| XM_011515752.1:c.1674G>A (CFTR) | XP_011514054.1:p.Glu558= | |
| XM_011515753.1:c.1341G>A (CFTR) | XP_011514055.1:p.Glu447= | |
| XM_011515754.1:c.1341G>A (CFTR) | XP_011514056.1:p.Glu447= | |
| NR_149084.1:n.221+1078C>T (CFTR-AS1) | ||
| NM_000492.4:c.1584G>A (CFTR) MANE Select | NP_000483.3:p.Glu528= |