Canonical Allele Identifier: CA327579
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 54008
ClinVar RCV Id: RCV001379902
dbSNP Id: rs397508760

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117534364_117534370del , CM000669.2:g.117534364_117534370del GRCh38
NC_000007.13:g.117174418_117174424del , CM000669.1:g.117174418_117174424del GRCh37
NC_000007.12:g.116961654_116961660del NCBI36
NG_016465.4:g.73581_73587del , LRG_663:g.73581_73587del

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.578_579+5del
ENST00000647978.2:c.*475_*476+5del
ENST00000649781.2:c.578_579+5del
ENST00000685018.2:c.578_579+5del
ENST00000687278.2:c.578_579+5del
ENST00000699585.1:c.578_579+5del
ENST00000699596.1:c.578_579+5del
ENST00000699597.1:c.578_579+5del
ENST00000699598.1:c.578_579+5del
ENST00000699599.1:c.578_579+5del
ENST00000699600.1:c.578_579+5del
ENST00000699601.1:c.578_579+5del
ENST00000699602.1:c.578_579+5del
ENST00000699604.1:c.*402_*403+5del
ENST00000699605.1:c.335_336+5del
ENST00000003084.11:c.578_579+5del
ENST00000647978.1:c.*475_*476+5del
ENST00000648260.1:c.578_579+5del
ENST00000649406.1:c.578_579+5del
ENST00000649781.1:c.578_579+5del
ENST00000673785.1:c.335_336+5del
ENST00000003084.10:c.578_579+5del
ENST00000426809.5:c.490-884_490-878del ENSP00000389119.1:n.490-884_490-878del
NM_000492.3:c.578_579+5del , LRG_663t1:c.578_579+5del
XM_011515751.1:c.668_669+5del
XM_011515752.1:c.668_669+5del
XM_011515753.1:c.335_336+5del
XM_011515754.1:c.335_336+5del
NM_000492.4:c.578_579+5del