Canonical Allele Identifier: CA1737422120
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117664812A= , CM000669.2:g.117664812A= GRCh38
NC_000007.13:g.117304866A= , CM000669.1:g.117304866A= GRCh37
NC_000007.12:g.117092102A= NCBI36
NG_016465.4:g.204029A= , LRG_663:g.204029A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.*297A= ENSP00000497673.2:n.*297A=
ENST00000647978.2:c.*3802A= ENSP00000497658.1:n.*3802A=
ENST00000649781.2:c.3905A= ENSP00000497203.1:p.Lys1302=
ENST00000685018.2:c.*301A= ENSP00000510194.2:n.*301A=
ENST00000687278.2:c.*741A= ENSP00000509593.2:n.*741A=
ENST00000699585.1:c.*297A= ENSP00000514456.1:n.*297A=
ENST00000699598.1:c.4088A= ENSP00000514467.1:p.Lys1363=
ENST00000699599.1:c.*301A= ENSP00000514468.1:n.*301A=
ENST00000699600.1:c.*749A= ENSP00000514469.1:n.*749A=
ENST00000699601.1:c.*2463A= ENSP00000514470.1:n.*2463A=
ENST00000699602.1:c.4082A= ENSP00000514471.1:p.Lys1361=
ENST00000699604.1:c.*3912A= ENSP00000514472.1:n.*3912A=
ENST00000699605.1:c.3662A= ENSP00000514473.1:p.Lys1221=
ENST00000699606.1:n.2256A=
ENST00000685018.1:c.952A= ENSP00000510194.1:n.952A=
ENST00000687278.1:c.1875A= ENSP00000509593.1:n.1875A=
ENST00000689011.1:c.670A=
ENST00000003084.11:c.4088A= MANE Select ENSP00000003084.6:p.Lys1363=
ENST00000647720.1:c.1538A=
ENST00000649781.1:c.3905A= ENSP00000497203.1:p.Lys1302=
ENST00000003084.10:c.4088A= ENSP00000003084.6:p.Lys1363=
ENST00000426809.5:c.3998A= ENSP00000389119.1:p.Lys1333=
ENST00000600166.1:c.214A=
NM_000492.3:c.4088A= , LRG_663t1:c.4088A= NP_000483.3:p.Lys1363=
XM_011515751.1:c.4178A= XP_011514053.1:p.Lys1393=
XM_011515752.1:c.4178A= XP_011514054.1:p.Lys1393=
XM_011515753.1:c.3845A= XP_011514055.1:p.Lys1282=
XM_011515754.1:c.3845A= XP_011514056.1:p.Lys1282=
NM_000492.4:c.4088A= MANE Select NP_000483.3:p.Lys1363=