Canonical Allele Identifier: CA1737423006
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117665552C= , CM000669.2:g.117665552C= GRCh38
NC_000007.13:g.117305606C= , CM000669.1:g.117305606C= GRCh37
NC_000007.12:g.117092842C= NCBI36
NG_016465.4:g.204769C= , LRG_663:g.204769C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.*439C= ENSP00000497673.2:n.*439C=
ENST00000647978.2:c.*3944C= ENSP00000497658.1:n.*3944C=
ENST00000649781.2:c.4047C= ENSP00000497203.1:p.Cys1349=
ENST00000685018.2:c.*443C= ENSP00000510194.2:n.*443C=
ENST00000687278.2:c.*883C= ENSP00000509593.2:n.*883C=
ENST00000699585.1:c.*439C= ENSP00000514456.1:n.*439C=
ENST00000699598.1:c.4230C= ENSP00000514467.1:p.Cys1410=
ENST00000699599.1:c.*443C= ENSP00000514468.1:n.*443C=
ENST00000699600.1:c.*891C= ENSP00000514469.1:n.*891C=
ENST00000699601.1:c.*2605C= ENSP00000514470.1:n.*2605C=
ENST00000699602.1:c.4224C= ENSP00000514471.1:p.Cys1408=
ENST00000699604.1:c.*4054C= ENSP00000514472.1:n.*4054C=
ENST00000699605.1:c.3804C= ENSP00000514473.1:p.Cys1268=
ENST00000699606.1:n.2398C=
ENST00000685018.1:c.1094C= ENSP00000510194.1:n.1094C=
ENST00000687278.1:c.2017C= ENSP00000509593.1:n.2017C=
ENST00000689011.1:c.812C=
ENST00000003084.11:c.4230C= MANE Select ENSP00000003084.6:p.Cys1410=
ENST00000647720.1:c.1680C=
ENST00000649781.1:c.4047C= ENSP00000497203.1:p.Cys1349=
ENST00000003084.10:c.4230C= ENSP00000003084.6:p.Cys1410=
ENST00000426809.5:c.4140C= ENSP00000389119.1:p.Cys1380=
ENST00000600166.1:c.356C=
NM_000492.3:c.4230C= , LRG_663t1:c.4230C= NP_000483.3:p.Cys1410=
XM_011515751.1:c.4320C= XP_011514053.1:p.Cys1440=
XM_011515752.1:c.4320C= XP_011514054.1:p.Cys1440=
XM_011515753.1:c.3987C= XP_011514055.1:p.Cys1329=
XM_011515754.1:c.3987C= XP_011514056.1:p.Cys1329=
NM_000492.4:c.4230C= MANE Select NP_000483.3:p.Cys1410=