Canonical Allele Identifier: CA1737422781
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117665466C= , CM000669.2:g.117665466C= GRCh38
NC_000007.13:g.117305520C= , CM000669.1:g.117305520C= GRCh37
NC_000007.12:g.117092756C= NCBI36
NG_016465.4:g.204683C= , LRG_663:g.204683C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.*353C= ENSP00000497673.2:n.*353C=
ENST00000647978.2:c.*3858C= ENSP00000497658.1:n.*3858C=
ENST00000649781.2:c.3961C= ENSP00000497203.1:p.Gln1321=
ENST00000685018.2:c.*357C= ENSP00000510194.2:n.*357C=
ENST00000687278.2:c.*797C= ENSP00000509593.2:n.*797C=
ENST00000699585.1:c.*353C= ENSP00000514456.1:n.*353C=
ENST00000699598.1:c.4144C= ENSP00000514467.1:p.Gln1382=
ENST00000699599.1:c.*357C= ENSP00000514468.1:n.*357C=
ENST00000699600.1:c.*805C= ENSP00000514469.1:n.*805C=
ENST00000699601.1:c.*2519C= ENSP00000514470.1:n.*2519C=
ENST00000699602.1:c.4138C= ENSP00000514471.1:p.Gln1380=
ENST00000699604.1:c.*3968C= ENSP00000514472.1:n.*3968C=
ENST00000699605.1:c.3718C= ENSP00000514473.1:p.Gln1240=
ENST00000699606.1:n.2312C=
ENST00000685018.1:c.1008C= ENSP00000510194.1:n.1008C=
ENST00000687278.1:c.1931C= ENSP00000509593.1:n.1931C=
ENST00000689011.1:c.726C=
ENST00000003084.11:c.4144C= MANE Select ENSP00000003084.6:p.Gln1382=
ENST00000647720.1:c.1594C=
ENST00000649781.1:c.3961C= ENSP00000497203.1:p.Gln1321=
ENST00000003084.10:c.4144C= ENSP00000003084.6:p.Gln1382=
ENST00000426809.5:c.4054C= ENSP00000389119.1:p.Gln1352=
ENST00000600166.1:c.270C=
NM_000492.3:c.4144C= , LRG_663t1:c.4144C= NP_000483.3:p.Gln1382=
XM_011515751.1:c.4234C= XP_011514053.1:p.Gln1412=
XM_011515752.1:c.4234C= XP_011514054.1:p.Gln1412=
XM_011515753.1:c.3901C= XP_011514055.1:p.Gln1301=
XM_011515754.1:c.3901C= XP_011514056.1:p.Gln1301=
NM_000492.4:c.4144C= MANE Select NP_000483.3:p.Gln1382=