Canonical Allele Identifier: CA1139660229
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 928746
dbSNP Id: rs1792031758

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117591968del , CM000669.2:g.117591968del GRCh38
NC_000007.13:g.117232022del , CM000669.1:g.117232022del GRCh37
NC_000007.12:g.117019258del NCBI36
NG_016465.4:g.131185del , LRG_663:g.131185del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.1801del ENSP00000497673.2:p.Ile601PhefsTer10
ENST00000647978.2:c.*1515del ENSP00000497658.1:n.*1515del
ENST00000649781.2:c.1618del ENSP00000497203.1:p.Ile540PhefsTer10
ENST00000685018.2:c.1801del ENSP00000510194.2:p.Ile601PhefsTer10
ENST00000687278.2:c.1801del ENSP00000509593.2:p.Ile601PhefsTer10
ENST00000699585.1:c.1801del ENSP00000514456.1:p.Ile601PhefsTer10
ENST00000699598.1:c.1801del ENSP00000514467.1:p.Ile601PhefsTer10
ENST00000699599.1:c.1801del ENSP00000514468.1:p.Ile601PhefsTer10
ENST00000699600.1:c.1801del ENSP00000514469.1:p.Ile601PhefsTer10
ENST00000699601.1:c.*101del ENSP00000514470.1:n.*101del
ENST00000699602.1:c.1801del ENSP00000514471.1:p.Ile601PhefsTer10
ENST00000699604.1:c.*1625del ENSP00000514472.1:n.*1625del
ENST00000699605.1:c.1375del ENSP00000514473.1:p.Ile459PhefsTer10
ENST00000003084.11:c.1801del MANE Select ENSP00000003084.6:p.Ile601PhefsTer10
ENST00000647978.1:c.*1515del ENSP00000497658.1:n.*1515del
ENST00000648260.1:c.1402-10858del ENSP00000497957.1:n.1402-10858del
ENST00000649406.1:c.1618del ENSP00000497965.1:p.Ile540PhefsTer10
ENST00000649781.1:c.1618del ENSP00000497203.1:p.Ile540PhefsTer10
ENST00000003084.10:c.1801del ENSP00000003084.6:p.Ile601PhefsTer10
ENST00000426809.5:c.1711del ENSP00000389119.1:p.Ile571PhefsTer10
NM_000492.3:c.1801del , LRG_663t1:c.1801del NP_000483.3:p.Ile601PhefsTer10
XM_011515751.1:c.1891del XP_011514053.1:p.Ile631PhefsTer10
XM_011515752.1:c.1891del XP_011514054.1:p.Ile631PhefsTer10
XM_011515753.1:c.1558del XP_011514055.1:p.Ile520PhefsTer10
XM_011515754.1:c.1558del XP_011514056.1:p.Ile520PhefsTer10
NM_000492.4:c.1801del MANE Select NP_000483.3:p.Ile601PhefsTer10