Canonical Allele Identifier: CA1737422146
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117664819G= , CM000669.2:g.117664819G= GRCh38
NC_000007.13:g.117304873G= , CM000669.1:g.117304873G= GRCh37
NC_000007.12:g.117092109G= NCBI36
NG_016465.4:g.204036G= , LRG_663:g.204036G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.*304G= ENSP00000497673.2:n.*304G=
ENST00000647978.2:c.*3809G= ENSP00000497658.1:n.*3809G=
ENST00000649781.2:c.3912G= ENSP00000497203.1:p.Lys1304=
ENST00000685018.2:c.*308G= ENSP00000510194.2:n.*308G=
ENST00000687278.2:c.*748G= ENSP00000509593.2:n.*748G=
ENST00000699585.1:c.*304G= ENSP00000514456.1:n.*304G=
ENST00000699598.1:c.4095G= ENSP00000514467.1:p.Lys1365=
ENST00000699599.1:c.*308G= ENSP00000514468.1:n.*308G=
ENST00000699600.1:c.*756G= ENSP00000514469.1:n.*756G=
ENST00000699601.1:c.*2470G= ENSP00000514470.1:n.*2470G=
ENST00000699602.1:c.4089G= ENSP00000514471.1:p.Lys1363=
ENST00000699604.1:c.*3919G= ENSP00000514472.1:n.*3919G=
ENST00000699605.1:c.3669G= ENSP00000514473.1:p.Lys1223=
ENST00000699606.1:n.2263G=
ENST00000685018.1:c.959G= ENSP00000510194.1:n.959G=
ENST00000687278.1:c.1882G= ENSP00000509593.1:n.1882G=
ENST00000689011.1:c.677G=
ENST00000003084.11:c.4095G= MANE Select ENSP00000003084.6:p.Lys1365=
ENST00000647720.1:c.1545G=
ENST00000649781.1:c.3912G= ENSP00000497203.1:p.Lys1304=
ENST00000003084.10:c.4095G= ENSP00000003084.6:p.Lys1365=
ENST00000426809.5:c.4005G= ENSP00000389119.1:p.Lys1335=
ENST00000600166.1:c.221G=
NM_000492.3:c.4095G= , LRG_663t1:c.4095G= NP_000483.3:p.Lys1365=
XM_011515751.1:c.4185G= XP_011514053.1:p.Lys1395=
XM_011515752.1:c.4185G= XP_011514054.1:p.Lys1395=
XM_011515753.1:c.3852G= XP_011514055.1:p.Lys1284=
XM_011515754.1:c.3852G= XP_011514056.1:p.Lys1284=
NM_000492.4:c.4095G= MANE Select NP_000483.3:p.Lys1365=