Canonical Allele Identifier: CA264801
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 66102
dbSNP Id: rs397515498

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117592620del , CM000669.2:g.117592620del GRCh38
NC_000007.13:g.117232674del , CM000669.1:g.117232674del GRCh37
NC_000007.12:g.117019910del NCBI36
NG_016465.4:g.131837del , LRG_663:g.131837del

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.2453del ENSP00000497673.2:p.Leu818TrpfsTer3
ENST00000647978.2:c.*2167del ENSP00000497658.1:n.*2167del
ENST00000649781.2:c.2270del ENSP00000497203.1:p.Leu757TrpfsTer3
ENST00000685018.2:c.2453del ENSP00000510194.2:p.Leu818TrpfsTer3
ENST00000687278.2:c.2453del ENSP00000509593.2:p.Leu818TrpfsTer3
ENST00000699585.1:c.2453del ENSP00000514456.1:p.Leu818TrpfsTer3
ENST00000699598.1:c.2453del ENSP00000514467.1:p.Leu818TrpfsTer3
ENST00000699599.1:c.2453del ENSP00000514468.1:p.Leu818TrpfsTer3
ENST00000699600.1:c.2453del ENSP00000514469.1:p.Leu818TrpfsTer3
ENST00000699601.1:c.*753del ENSP00000514470.1:n.*753del
ENST00000699602.1:c.2453del ENSP00000514471.1:p.Leu818TrpfsTer3
ENST00000699604.1:c.*2277del ENSP00000514472.1:n.*2277del
ENST00000699605.1:c.2027del ENSP00000514473.1:p.Leu676TrpfsTer3
ENST00000687278.1:c.44del ENSP00000509593.1:p.Leu15TrpfsTer3
ENST00000003084.11:c.2453del MANE Select ENSP00000003084.6:p.Leu818TrpfsTer3
ENST00000647720.1:c.103del
ENST00000647978.1:c.*2167del ENSP00000497658.1:n.*2167del
ENST00000648260.1:c.1402-10206del ENSP00000497957.1:n.1402-10206del
ENST00000649406.1:c.2270del ENSP00000497965.1:p.Leu757TrpfsTer3
ENST00000649781.1:c.2270del ENSP00000497203.1:p.Leu757TrpfsTer3
ENST00000003084.10:c.2453del ENSP00000003084.6:p.Leu818TrpfsTer3
ENST00000426809.5:c.2363del ENSP00000389119.1:p.Leu788TrpfsTer3
NM_000492.3:c.2453del , LRG_663t1:c.2453del NP_000483.3:p.Leu818TrpfsTer3
XM_011515751.1:c.2543del XP_011514053.1:p.Leu848TrpfsTer3
XM_011515752.1:c.2543del XP_011514054.1:p.Leu848TrpfsTer3
XM_011515753.1:c.2210del XP_011514055.1:p.Leu737TrpfsTer3
XM_011515754.1:c.2210del XP_011514056.1:p.Leu737TrpfsTer3
NM_000492.4:c.2453del MANE Select NP_000483.3:p.Leu818TrpfsTer3