Canonical Allele Identifier: CA1737404772
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117642511A= , CM000669.2:g.117642511A= GRCh38
NC_000007.13:g.117282565A= , CM000669.1:g.117282565A= GRCh37
NC_000007.12:g.117069801A= NCBI36
NG_016465.4:g.181728A= , LRG_663:g.181728A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.3591A= ENSP00000497673.2:p.Ter1197=
ENST00000647978.2:c.*3505A= ENSP00000497658.1:n.*3505A=
ENST00000649781.2:c.3608A= ENSP00000497203.1:p.Glu1203=
ENST00000685018.2:c.3791A= ENSP00000510194.2:p.Glu1264=
ENST00000687278.2:c.*444A= ENSP00000509593.2:n.*444A=
ENST00000699585.1:c.3591A= ENSP00000514456.1:p.Ter1197=
ENST00000699598.1:c.3791A= ENSP00000514467.1:p.Glu1264=
ENST00000699599.1:c.3791A= ENSP00000514468.1:p.Glu1264=
ENST00000699600.1:c.*452A= ENSP00000514469.1:n.*452A=
ENST00000699601.1:c.*2166A= ENSP00000514470.1:n.*2166A=
ENST00000699602.1:c.3785A= ENSP00000514471.1:p.Glu1262=
ENST00000699604.1:c.*3615A= ENSP00000514472.1:n.*3615A=
ENST00000699605.1:c.3365A= ENSP00000514473.1:p.Glu1122=
ENST00000685018.1:c.539A= ENSP00000510194.1:p.Glu180=
ENST00000687278.1:c.1578A= ENSP00000509593.1:n.1578A=
ENST00000689011.1:c.373A=
ENST00000003084.11:c.3791A= MANE Select ENSP00000003084.6:p.Glu1264=
ENST00000647720.1:c.1241A=
ENST00000649781.1:c.3608A= ENSP00000497203.1:p.Glu1203=
ENST00000003084.10:c.3791A= ENSP00000003084.6:p.Glu1264=
ENST00000426809.5:c.3701A= ENSP00000389119.1:p.Glu1234=
NM_000492.3:c.3791A= , LRG_663t1:c.3791A= NP_000483.3:p.Glu1264=
XM_011515751.1:c.3881A= XP_011514053.1:p.Glu1294=
XM_011515752.1:c.3881A= XP_011514054.1:p.Glu1294=
XM_011515753.1:c.3548A= XP_011514055.1:p.Glu1183=
XM_011515754.1:c.3548A= XP_011514056.1:p.Glu1183=
NM_000492.4:c.3791A= MANE Select NP_000483.3:p.Glu1264=