Canonical Allele Identifier: CA326791
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 53473
ClinVar RCV Id: RCV001009458
dbSNP Id: rs397508364

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117592491_117592492del , CM000669.2:g.117592491_117592492del GRCh38
NC_000007.13:g.117232545_117232546del , CM000669.1:g.117232545_117232546del GRCh37
NC_000007.12:g.117019781_117019782del NCBI36
NG_016465.4:g.131708_131709del , LRG_663:g.131708_131709del

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.2324_2325del ENSP00000497673.2:p.His775LeufsTer3
ENST00000647978.2:c.*2038_*2039del ENSP00000497658.1:n.*2038_*2039del
ENST00000649781.2:c.2141_2142del ENSP00000497203.1:p.His714LeufsTer3
ENST00000685018.2:c.2324_2325del ENSP00000510194.2:p.His775LeufsTer3
ENST00000687278.2:c.2324_2325del ENSP00000509593.2:p.His775LeufsTer3
ENST00000699585.1:c.2324_2325del ENSP00000514456.1:p.His775LeufsTer3
ENST00000699598.1:c.2324_2325del ENSP00000514467.1:p.His775LeufsTer3
ENST00000699599.1:c.2324_2325del ENSP00000514468.1:p.His775LeufsTer3
ENST00000699600.1:c.2324_2325del ENSP00000514469.1:p.His775LeufsTer3
ENST00000699601.1:c.*624_*625del ENSP00000514470.1:n.*624_*625del
ENST00000699602.1:c.2324_2325del ENSP00000514471.1:p.His775LeufsTer3
ENST00000699604.1:c.*2148_*2149del ENSP00000514472.1:n.*2148_*2149del
ENST00000699605.1:c.1898_1899del ENSP00000514473.1:p.His633LeufsTer3
ENST00000003084.11:c.2324_2325del MANE Select ENSP00000003084.6:p.His775LeufsTer3
ENST00000647978.1:c.*2038_*2039del ENSP00000497658.1:n.*2038_*2039del
ENST00000648260.1:c.1402-10335_1402-10334del ENSP00000497957.1:n.1402-10335_1402-10334del
ENST00000649406.1:c.2141_2142del ENSP00000497965.1:p.His714LeufsTer3
ENST00000649781.1:c.2141_2142del ENSP00000497203.1:p.His714LeufsTer3
ENST00000003084.10:c.2324_2325del ENSP00000003084.6:p.His775LeufsTer3
ENST00000426809.5:c.2234_2235del ENSP00000389119.1:p.His745LeufsTer3
NM_000492.3:c.2324_2325del , LRG_663t1:c.2324_2325del NP_000483.3:p.His775LeufsTer3
XM_011515751.1:c.2414_2415del XP_011514053.1:p.His805LeufsTer3
XM_011515752.1:c.2414_2415del XP_011514054.1:p.His805LeufsTer3
XM_011515753.1:c.2081_2082del XP_011514055.1:p.His694LeufsTer3
XM_011515754.1:c.2081_2082del XP_011514056.1:p.His694LeufsTer3
NM_000492.4:c.2324_2325del MANE Select NP_000483.3:p.His775LeufsTer3