Canonical Allele Identifier: CA1737361633
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117534126_117534127delinsAG , CM000669.2:g.117534126_117534127delinsAG GRCh38
NC_000007.13:g.117174180_117174181delinsAG , CM000669.1:g.117174180_117174181delinsAG GRCh37
NC_000007.12:g.116961416_116961417delinsAG NCBI36
NG_016465.4:g.73343_73344delinsAG , LRG_663:g.73343_73344delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.490-150_490-149delinsAG ENSP00000497673.2:n.490-150_490-149delins...
ENST00000647978.2:c.*387-150_*387-149delinsAG ENSP00000497658.1:n.*387-150_*387-149deli...
ENST00000649781.2:c.490-150_490-149delinsAG ENSP00000497203.1:n.490-150_490-149delins...
ENST00000685018.2:c.490-150_490-149delinsAG ENSP00000510194.2:n.490-150_490-149delins...
ENST00000687278.2:c.490-150_490-149delinsAG ENSP00000509593.2:n.490-150_490-149delins...
ENST00000699585.1:c.490-150_490-149delinsAG ENSP00000514456.1:n.490-150_490-149delins...
ENST00000699596.1:c.490-150_490-149delinsAG ENSP00000514465.1:n.490-150_490-149delins...
ENST00000699597.1:c.490-150_490-149delinsAG ENSP00000514466.1:n.490-150_490-149delins...
ENST00000699598.1:c.490-150_490-149delinsAG ENSP00000514467.1:n.490-150_490-149delins...
ENST00000699599.1:c.490-150_490-149delinsAG ENSP00000514468.1:n.490-150_490-149delins...
ENST00000699600.1:c.490-150_490-149delinsAG ENSP00000514469.1:n.490-150_490-149delins...
ENST00000699601.1:c.490-150_490-149delinsAG ENSP00000514470.1:n.490-150_490-149delins...
ENST00000699602.1:c.490-150_490-149delinsAG ENSP00000514471.1:n.490-150_490-149delins...
ENST00000699604.1:c.*314-150_*314-149delinsAG ENSP00000514472.1:n.*314-150_*314-149deli...
ENST00000699605.1:c.247-150_247-149delinsAG ENSP00000514473.1:n.247-150_247-149delins...
ENST00000003084.11:c.490-150_490-149delinsAG MANE Select ENSP00000003084.6:n.490-150_490-149delins...
ENST00000647978.1:c.*387-150_*387-149delinsAG ENSP00000497658.1:n.*387-150_*387-149deli...
ENST00000648260.1:c.490-150_490-149delinsAG ENSP00000497957.1:n.490-150_490-149delins...
ENST00000649406.1:c.490-150_490-149delinsAG ENSP00000497965.1:n.490-150_490-149delins...
ENST00000649781.1:c.490-150_490-149delinsAG ENSP00000497203.1:n.490-150_490-149delins...
ENST00000673785.1:c.247-150_247-149delinsAG ENSP00000501235.1:n.247-150_247-149delins...
ENST00000003084.10:c.490-150_490-149delinsAG ENSP00000003084.6:n.490-150_490-149delins...
ENST00000426809.5:c.490-1122_490-1121delinsAG ENSP00000389119.1:n.490-1122_490-1121deli...
NM_000492.3:c.490-150_490-149delinsAG , LRG_663t1:c.490-150_490-149delinsAG NP_000483.3:n.490-150_490-149delinsAG
XM_011515751.1:c.580-150_580-149delinsAG XP_011514053.1:n.580-150_580-149delinsAG
XM_011515752.1:c.580-150_580-149delinsAG XP_011514054.1:n.580-150_580-149delinsAG
XM_011515753.1:c.247-150_247-149delinsAG XP_011514055.1:n.247-150_247-149delinsAG
XM_011515754.1:c.247-150_247-149delinsAG XP_011514056.1:n.247-150_247-149delinsAG
NM_000492.4:c.490-150_490-149delinsAG MANE Select NP_000483.3:n.490-150_490-149delinsAG