Canonical Allele Identifier: CA368979764
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 2446883
ClinVar RCV Id: RCV003159583

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117542015G>T , CM000669.2:g.117542015G>T GRCh38
NC_000007.13:g.117182069G>T , CM000669.1:g.117182069G>T GRCh37
NC_000007.12:g.116969305G>T NCBI36
NG_016465.4:g.81232G>T , LRG_663:g.81232G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.1117-1G>T ENSP00000497673.2:n.1117-1G>T
ENST00000647978.2:c.*1014-1G>T ENSP00000497658.1:n.*1014-1G>T
ENST00000649781.2:c.1117-1G>T ENSP00000497203.1:n.1117-1G>T
ENST00000685018.2:c.1117-1G>T ENSP00000510194.2:n.1117-1G>T
ENST00000687278.2:c.1117-1G>T ENSP00000509593.2:n.1117-1G>T
ENST00000699585.1:c.1117-1G>T ENSP00000514456.1:n.1117-1G>T
ENST00000699596.1:c.1117-1G>T ENSP00000514465.1:n.1117-1G>T
ENST00000699597.1:c.1117-1G>T ENSP00000514466.1:n.1117-1G>T
ENST00000699598.1:c.1117-1G>T ENSP00000514467.1:n.1117-1G>T
ENST00000699599.1:c.1117-1G>T ENSP00000514468.1:n.1117-1G>T
ENST00000699600.1:c.1117-1G>T ENSP00000514469.1:n.1117-1G>T
ENST00000699601.1:c.1117-1G>T ENSP00000514470.1:n.1117-1G>T
ENST00000699602.1:c.1117-1G>T ENSP00000514471.1:n.1117-1G>T
ENST00000699604.1:c.*941-1G>T ENSP00000514472.1:n.*941-1G>T
ENST00000699605.1:c.874-1G>T ENSP00000514473.1:n.874-1G>T
ENST00000003084.11:c.1117-1G>T MANE Select ENSP00000003084.6:n.1117-1G>T
ENST00000647978.1:c.*1014-1G>T ENSP00000497658.1:n.*1014-1G>T
ENST00000648260.1:c.1117-1G>T ENSP00000497957.1:n.1117-1G>T
ENST00000649406.1:c.1117-1G>T ENSP00000497965.1:n.1117-1G>T
ENST00000649781.1:c.1117-1G>T ENSP00000497203.1:n.1117-1G>T
ENST00000673785.1:c.874-1G>T ENSP00000501235.1:n.874-1G>T
ENST00000003084.10:c.1117-1G>T ENSP00000003084.6:n.1117-1G>T
ENST00000426809.5:c.1027-1G>T ENSP00000389119.1:n.1027-1G>T
NM_000492.3:c.1117-1G>T , LRG_663t1:c.1117-1G>T NP_000483.3:n.1117-1G>T
XM_011515751.1:c.1207-1G>T XP_011514053.1:n.1207-1G>T
XM_011515752.1:c.1207-1G>T XP_011514054.1:n.1207-1G>T
XM_011515753.1:c.874-1G>T XP_011514055.1:n.874-1G>T
XM_011515754.1:c.874-1G>T XP_011514056.1:n.874-1G>T
NM_000492.4:c.1117-1G>T MANE Select NP_000483.3:n.1117-1G>T