Canonical Allele Identifier: CA1737374083
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117603348_117603349delinsAT , CM000669.2:g.117603348_117603349delinsAT GRCh38
NC_000007.13:g.117243402_117243403delinsAT , CM000669.1:g.117243402_117243403delinsAT GRCh37
NC_000007.12:g.117030638_117030639delinsAT NCBI36
NG_016465.4:g.142565_142566delinsAT , LRG_663:g.142565_142566delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.2658-184_2658-183delinsAT ENSP00000497673.2:n.2658-184_2658-183delinsAT
ENST00000647978.2:c.*2372-184_*2372-183delinsAT ENSP00000497658.1:n.*2372-184_*2372-183delinsAT
ENST00000649781.2:c.2475-184_2475-183delinsAT ENSP00000497203.1:n.2475-184_2475-183delinsAT
ENST00000685018.2:c.2658-184_2658-183delinsAT ENSP00000510194.2:n.2658-184_2658-183delinsAT
ENST00000687278.2:c.2658-184_2658-183delinsAT ENSP00000509593.2:n.2658-184_2658-183delinsAT
ENST00000699585.1:c.2658-184_2658-183delinsAT ENSP00000514456.1:n.2658-184_2658-183delinsAT
ENST00000699598.1:c.2658-184_2658-183delinsAT ENSP00000514467.1:n.2658-184_2658-183delinsAT
ENST00000699599.1:c.2658-184_2658-183delinsAT ENSP00000514468.1:n.2658-184_2658-183delinsAT
ENST00000699600.1:c.2658-184_2658-183delinsAT ENSP00000514469.1:n.2658-184_2658-183delinsAT
ENST00000699601.1:c.*958-184_*958-183delinsAT ENSP00000514470.1:n.*958-184_*958-183delinsAT
ENST00000699602.1:c.2658-184_2658-183delinsAT ENSP00000514471.1:n.2658-184_2658-183delinsAT
ENST00000699604.1:c.*2482-184_*2482-183delinsAT ENSP00000514472.1:n.*2482-184_*2482-183delinsAT
ENST00000699605.1:c.2232-184_2232-183delinsAT ENSP00000514473.1:n.2232-184_2232-183delinsAT
ENST00000687278.1:c.249-184_249-183delinsAT ENSP00000509593.1:n.249-184_249-183delinsAT
ENST00000003084.11:c.2658-184_2658-183delinsAT MANE Select ENSP00000003084.6:n.2658-184_2658-183delinsAT
ENST00000647720.1:c.308-184_308-183delinsAT
ENST00000648260.1:c.1440-184_1440-183delinsAT ENSP00000497957.1:n.1440-184_1440-183delinsAT
ENST00000649406.1:c.2475-184_2475-183delinsAT ENSP00000497965.1:n.2475-184_2475-183delinsAT
ENST00000649781.1:c.2475-184_2475-183delinsAT ENSP00000497203.1:n.2475-184_2475-183delinsAT
ENST00000003084.10:c.2658-184_2658-183delinsAT ENSP00000003084.6:n.2658-184_2658-183delinsAT
ENST00000426809.5:c.2568-184_2568-183delinsAT ENSP00000389119.1:n.2568-184_2568-183delinsAT
NM_000492.3:c.2658-184_2658-183delinsAT , LRG_663t1:c.2658-184_2658-183delinsAT NP_000483.3:n.2658-184_2658-183delinsAT
XM_011515751.1:c.2748-184_2748-183delinsAT XP_011514053.1:n.2748-184_2748-183delinsAT
XM_011515752.1:c.2748-184_2748-183delinsAT XP_011514054.1:n.2748-184_2748-183delinsAT
XM_011515753.1:c.2415-184_2415-183delinsAT XP_011514055.1:n.2415-184_2415-183delinsAT
XM_011515754.1:c.2415-184_2415-183delinsAT XP_011514056.1:n.2415-184_2415-183delinsAT
NM_000492.4:c.2658-184_2658-183delinsAT MANE Select NP_000483.3:n.2658-184_2658-183delinsAT