Canonical Allele Identifier: CA2695208503
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117592020_117592030del , CM000669.2:g.117592020_117592030del GRCh38
NC_000007.13:g.117232074_117232084del , CM000669.1:g.117232074_117232084del GRCh37
NC_000007.12:g.117019310_117019320del NCBI36
NG_016465.4:g.131237_131247del , LRG_663:g.131237_131247del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.1853_1863del ENSP00000497673.2:p.Ile618ArgfsTer2
ENST00000647978.2:c.*1567_*1577del ENSP00000497658.1:n.*1567_*1577del
ENST00000649781.2:c.1670_1680del ENSP00000497203.1:p.Ile557ArgfsTer2
ENST00000685018.2:c.1853_1863del ENSP00000510194.2:p.Ile618ArgfsTer2
ENST00000687278.2:c.1853_1863del ENSP00000509593.2:p.Ile618ArgfsTer2
ENST00000699585.1:c.1853_1863del ENSP00000514456.1:p.Ile618ArgfsTer2
ENST00000699598.1:c.1853_1863del ENSP00000514467.1:p.Ile618ArgfsTer2
ENST00000699599.1:c.1853_1863del ENSP00000514468.1:p.Ile618ArgfsTer2
ENST00000699600.1:c.1853_1863del ENSP00000514469.1:p.Ile618ArgfsTer2
ENST00000699601.1:c.*153_*163del ENSP00000514470.1:n.*153_*163del
ENST00000699602.1:c.1853_1863del ENSP00000514471.1:p.Ile618ArgfsTer2
ENST00000699604.1:c.*1677_*1687del ENSP00000514472.1:n.*1677_*1687del
ENST00000699605.1:c.1427_1437del ENSP00000514473.1:p.Ile476ArgfsTer2
ENST00000003084.11:c.1853_1863del MANE Select ENSP00000003084.6:p.Ile618ArgfsTer2
ENST00000647978.1:c.*1567_*1577del ENSP00000497658.1:n.*1567_*1577del
ENST00000648260.1:c.1402-10806_1402-10796del ENSP00000497957.1:n.1402-10806_1402-10796del
ENST00000649406.1:c.1670_1680del ENSP00000497965.1:p.Ile557ArgfsTer2
ENST00000649781.1:c.1670_1680del ENSP00000497203.1:p.Ile557ArgfsTer2
ENST00000003084.10:c.1853_1863del ENSP00000003084.6:p.Ile618ArgfsTer2
ENST00000426809.5:c.1763_1773del ENSP00000389119.1:p.Ile588ArgfsTer2
NM_000492.3:c.1853_1863del , LRG_663t1:c.1853_1863del NP_000483.3:p.Ile618ArgfsTer2
XM_011515751.1:c.1943_1953del XP_011514053.1:p.Ile648ArgfsTer2
XM_011515752.1:c.1943_1953del XP_011514054.1:p.Ile648ArgfsTer2
XM_011515753.1:c.1610_1620del XP_011514055.1:p.Ile537ArgfsTer2
XM_011515754.1:c.1610_1620del XP_011514056.1:p.Ile537ArgfsTer2
NM_000492.4:c.1853_1863del MANE Select NP_000483.3:p.Ile618ArgfsTer2