Canonical Allele Identifier: CA326929
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53570
ClinVar RCV Id: RCV000577697
dbSNP Id: rs397508437

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117603673A>T , CM000669.2:g.117603673A>T GRCh38
NC_000007.13:g.117243727A>T , CM000669.1:g.117243727A>T GRCh37
NC_000007.12:g.117030963A>T NCBI36
NG_016465.4:g.142890A>T , LRG_663:g.142890A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.2799A>T ENSP00000497673.2:p.Arg933Ser
ENST00000647978.2:c.*2513A>T ENSP00000497658.1:n.*2513A>T
ENST00000649781.2:c.2616A>T ENSP00000497203.1:p.Arg872Ser
ENST00000685018.2:c.2799A>T ENSP00000510194.2:p.Arg933Ser
ENST00000687278.2:c.2799A>T ENSP00000509593.2:p.Arg933Ser
ENST00000699585.1:c.2799A>T ENSP00000514456.1:p.Arg933Ser
ENST00000699598.1:c.2799A>T ENSP00000514467.1:p.Arg933Ser
ENST00000699599.1:c.2799A>T ENSP00000514468.1:p.Arg933Ser
ENST00000699600.1:c.2799A>T ENSP00000514469.1:p.Arg933Ser
ENST00000699601.1:c.*1099A>T ENSP00000514470.1:n.*1099A>T
ENST00000699602.1:c.2799A>T ENSP00000514471.1:p.Arg933Ser
ENST00000699604.1:c.*2623A>T ENSP00000514472.1:n.*2623A>T
ENST00000699605.1:c.2373A>T ENSP00000514473.1:p.Arg791Ser
ENST00000687278.1:c.390A>T ENSP00000509593.1:p.Arg130Ser
ENST00000003084.11:c.2799A>T MANE Select ENSP00000003084.6:p.Arg933Ser
ENST00000647720.1:c.449A>T
ENST00000648260.1:c.1581A>T ENSP00000497957.1:p.Arg527Ser
ENST00000649406.1:c.2616A>T ENSP00000497965.1:p.Arg872Ser
ENST00000649781.1:c.2616A>T ENSP00000497203.1:p.Arg872Ser
ENST00000003084.10:c.2799A>T ENSP00000003084.6:p.Arg933Ser
ENST00000426809.5:c.2709A>T ENSP00000389119.1:p.Arg903Ser
NM_000492.3:c.2799A>T , LRG_663t1:c.2799A>T NP_000483.3:p.Arg933Ser
XM_011515751.1:c.2889A>T XP_011514053.1:p.Arg963Ser
XM_011515752.1:c.2889A>T XP_011514054.1:p.Arg963Ser
XM_011515753.1:c.2556A>T XP_011514055.1:p.Arg852Ser
XM_011515754.1:c.2556A>T XP_011514056.1:p.Arg852Ser
NM_000492.4:c.2799A>T MANE Select NP_000483.3:p.Arg933Ser