Canonical Allele Identifier: CA1737404776
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117642517A= , CM000669.2:g.117642517A= GRCh38
NC_000007.13:g.117282571A= , CM000669.1:g.117282571A= GRCh37
NC_000007.12:g.117069807A= NCBI36
NG_016465.4:g.181734A= , LRG_663:g.181734A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.*6A= ENSP00000497673.2:n.*6A=
ENST00000647978.2:c.*3511A= ENSP00000497658.1:n.*3511A=
ENST00000649781.2:c.3614A= ENSP00000497203.1:p.Glu1205=
ENST00000685018.2:c.3797A= ENSP00000510194.2:p.Glu1266=
ENST00000687278.2:c.*450A= ENSP00000509593.2:n.*450A=
ENST00000699585.1:c.*6A= ENSP00000514456.1:n.*6A=
ENST00000699598.1:c.3797A= ENSP00000514467.1:p.Glu1266=
ENST00000699599.1:c.3797A= ENSP00000514468.1:p.Glu1266=
ENST00000699600.1:c.*458A= ENSP00000514469.1:n.*458A=
ENST00000699601.1:c.*2172A= ENSP00000514470.1:n.*2172A=
ENST00000699602.1:c.3791A= ENSP00000514471.1:p.Glu1264=
ENST00000699604.1:c.*3621A= ENSP00000514472.1:n.*3621A=
ENST00000699605.1:c.3371A= ENSP00000514473.1:p.Glu1124=
ENST00000685018.1:c.545A= ENSP00000510194.1:p.Glu182=
ENST00000687278.1:c.1584A= ENSP00000509593.1:n.1584A=
ENST00000689011.1:c.379A=
ENST00000003084.11:c.3797A= MANE Select ENSP00000003084.6:p.Glu1266=
ENST00000647720.1:c.1247A=
ENST00000649781.1:c.3614A= ENSP00000497203.1:p.Glu1205=
ENST00000003084.10:c.3797A= ENSP00000003084.6:p.Glu1266=
ENST00000426809.5:c.3707A= ENSP00000389119.1:p.Glu1236=
NM_000492.3:c.3797A= , LRG_663t1:c.3797A= NP_000483.3:p.Glu1266=
XM_011515751.1:c.3887A= XP_011514053.1:p.Glu1296=
XM_011515752.1:c.3887A= XP_011514054.1:p.Glu1296=
XM_011515753.1:c.3554A= XP_011514055.1:p.Glu1185=
XM_011515754.1:c.3554A= XP_011514056.1:p.Glu1185=
NM_000492.4:c.3797A= MANE Select NP_000483.3:p.Glu1266=