Canonical Allele Identifier: CA2777588389
Gene: CFTR HGNC NCBI
CFTR-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117548331_117548334del , CM000669.2:g.117548331_117548334del GRCh38
NC_000007.13:g.117188385_117188388del , CM000669.1:g.117188385_117188388del GRCh37
NC_000007.12:g.116975621_116975624del NCBI36
NG_016465.4:g.87548_87551del , LRG_663:g.87548_87551del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.1210-310_1210-307del (CFTR) ENSP00000497673.2:n.1210-310_1210-307del
ENST00000647978.2:c.*1106+6223_*1106+6226del (CFTR) ENSP00000497658.1:n.*1106+6223_*1106+6226del
ENST00000649781.2:c.1209+6223_1209+6226del (CFTR) ENSP00000497203.1:n.1209+6223_1209+6226del
ENST00000685018.2:c.1210-310_1210-307del (CFTR) ENSP00000510194.2:n.1210-310_1210-307del
ENST00000687278.2:c.1210-310_1210-307del (CFTR) ENSP00000509593.2:n.1210-310_1210-307del
ENST00000699585.1:c.1210-310_1210-307del (CFTR) ENSP00000514456.1:n.1210-310_1210-307del
ENST00000699596.1:c.1210-310_1210-307del (CFTR) ENSP00000514465.1:n.1210-310_1210-307del
ENST00000699597.1:c.1210-310_1210-307del (CFTR) ENSP00000514466.1:n.1210-310_1210-307del
ENST00000699598.1:c.1210-310_1210-307del (CFTR) ENSP00000514467.1:n.1210-310_1210-307del
ENST00000699599.1:c.1210-310_1210-307del (CFTR) ENSP00000514468.1:n.1210-310_1210-307del
ENST00000699600.1:c.1210-310_1210-307del (CFTR) ENSP00000514469.1:n.1210-310_1210-307del
ENST00000699601.1:c.1210-310_1210-307del (CFTR) ENSP00000514470.1:n.1210-310_1210-307del
ENST00000699602.1:c.1210-310_1210-307del (CFTR) ENSP00000514471.1:n.1210-310_1210-307del
ENST00000699604.1:c.*1034-310_*1034-307del (CFTR) ENSP00000514472.1:n.*1034-310_*1034-307del
ENST00000699605.1:c.966+6223_966+6226del (CFTR) ENSP00000514473.1:n.966+6223_966+6226del
ENST00000003084.11:c.1210-310_1210-307del (CFTR) MANE Select ENSP00000003084.6:n.1210-310_1210-307del
ENST00000647978.1:c.*1106+6223_*1106+6226del (CFTR) ENSP00000497658.1:n.*1106+6223_*1106+6226del
ENST00000648260.1:c.1209+6223_1209+6226del (CFTR) ENSP00000497957.1:n.1209+6223_1209+6226del
ENST00000649406.1:c.1209+6223_1209+6226del (CFTR) ENSP00000497965.1:n.1209+6223_1209+6226del
ENST00000649781.1:c.1209+6223_1209+6226del (CFTR) ENSP00000497203.1:n.1209+6223_1209+6226del
ENST00000673785.1:c.967-310_967-307del (CFTR) ENSP00000501235.1:n.967-310_967-307del
ENST00000003084.10:c.1210-310_1210-307del (CFTR) ENSP00000003084.6:n.1210-310_1210-307del
ENST00000426809.5:c.1120-310_1120-307del (CFTR) ENSP00000389119.1:n.1120-310_1120-307del
NM_000492.3:c.1210-310_1210-307del , LRG_663t1:c.1210-310_1210-307del (CFTR) NP_000483.3:n.1210-310_1210-307del
XM_011515751.1:c.1300-310_1300-307del (CFTR) XP_011514053.1:n.1300-310_1300-307del
XM_011515752.1:c.1300-310_1300-307del (CFTR) XP_011514054.1:n.1300-310_1300-307del
XM_011515753.1:c.967-310_967-307del (CFTR) XP_011514055.1:n.967-310_967-307del
XM_011515754.1:c.967-310_967-307del (CFTR) XP_011514056.1:n.967-310_967-307del
NR_149084.1:n.222-5794_222-5791del (CFTR-AS1)
NM_000492.4:c.1210-310_1210-307del (CFTR) MANE Select NP_000483.3:n.1210-310_1210-307del