Canonical Allele Identifier: CA340648
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 7168
dbSNP Id: rs121908748

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117590440G>A , CM000669.2:g.117590440G>A GRCh38
NC_000007.13:g.117230494G>A , CM000669.1:g.117230494G>A GRCh37
NC_000007.12:g.117017730G>A NCBI36
NG_016465.4:g.129657G>A , LRG_663:g.129657G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.1766+1G>A ENSP00000497673.2:n.1766+1G>A
ENST00000647978.2:c.*1480+1G>A ENSP00000497658.1:n.*1480+1G>A
ENST00000649781.2:c.1583+1G>A ENSP00000497203.1:n.1583+1G>A
ENST00000685018.2:c.1766+1G>A ENSP00000510194.2:n.1766+1G>A
ENST00000687278.2:c.1766+1G>A ENSP00000509593.2:n.1766+1G>A
ENST00000699585.1:c.1766+1G>A ENSP00000514456.1:n.1766+1G>A
ENST00000699598.1:c.1766+1G>A ENSP00000514467.1:n.1766+1G>A
ENST00000699599.1:c.1766+1G>A ENSP00000514468.1:n.1766+1G>A
ENST00000699600.1:c.1766+1G>A ENSP00000514469.1:n.1766+1G>A
ENST00000699601.1:c.*66+1G>A ENSP00000514470.1:n.*66+1G>A
ENST00000699602.1:c.1766+1G>A ENSP00000514471.1:n.1766+1G>A
ENST00000699604.1:c.*1590+1G>A ENSP00000514472.1:n.*1590+1G>A
ENST00000699605.1:c.1340+1G>A ENSP00000514473.1:n.1340+1G>A
ENST00000003084.11:c.1766+1G>A MANE Select ENSP00000003084.6:n.1766+1G>A
ENST00000647978.1:c.*1480+1G>A ENSP00000497658.1:n.*1480+1G>A
ENST00000648260.1:c.1402-12386G>A ENSP00000497957.1:n.1402-12386G>A
ENST00000649406.1:c.1583+1G>A ENSP00000497965.1:n.1583+1G>A
ENST00000649781.1:c.1583+1G>A ENSP00000497203.1:n.1583+1G>A
ENST00000003084.10:c.1766+1G>A ENSP00000003084.6:n.1766+1G>A
ENST00000426809.5:c.1676+1G>A ENSP00000389119.1:n.1676+1G>A
NM_000492.3:c.1766+1G>A , LRG_663t1:c.1766+1G>A NP_000483.3:n.1766+1G>A
XM_011515751.1:c.1856+1G>A XP_011514053.1:n.1856+1G>A
XM_011515752.1:c.1856+1G>A XP_011514054.1:n.1856+1G>A
XM_011515753.1:c.1523+1G>A XP_011514055.1:n.1523+1G>A
XM_011515754.1:c.1523+1G>A XP_011514056.1:n.1523+1G>A
NM_000492.4:c.1766+1G>A MANE Select NP_000483.3:n.1766+1G>A