Canonical Allele Identifier: CA1737404638

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117642212T= , CM000669.2:g.117642212T=	GRCh38
NC_000007.13:g.117282266T= , CM000669.1:g.117282266T=	GRCh37
NC_000007.12:g.117069502T=	NCBI36
NG_016465.4:g.181429T= , LRG_663:g.181429T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3518-226T=	ENSP00000497673.2:n.3518-226T=
ENST00000647978.2:c.*3432-226T=	ENSP00000497658.1:n.*3432-226T=
ENST00000649781.2:c.3535-226T=	ENSP00000497203.1:n.3535-226T=
ENST00000685018.2:c.3718-226T=	ENSP00000510194.2:n.3718-226T=
ENST00000687278.2:c.*371-226T=	ENSP00000509593.2:n.*371-226T=
ENST00000699585.1:c.3518-226T=	ENSP00000514456.1:n.3518-226T=
ENST00000699598.1:c.3718-226T=	ENSP00000514467.1:n.3718-226T=
ENST00000699599.1:c.3718-226T=	ENSP00000514468.1:n.3718-226T=
ENST00000699600.1:c.*379-226T=	ENSP00000514469.1:n.*379-226T=
ENST00000699601.1:c.*2093-226T=	ENSP00000514470.1:n.*2093-226T=
ENST00000699602.1:c.3712-226T=	ENSP00000514471.1:n.3712-226T=
ENST00000699604.1:c.*3542-226T=	ENSP00000514472.1:n.*3542-226T=
ENST00000699605.1:c.3292-226T=	ENSP00000514473.1:n.3292-226T=
ENST00000685018.1:c.466-226T=	ENSP00000510194.1:n.466-226T=
ENST00000687278.1:c.1505-226T=	ENSP00000509593.1:n.1505-226T=
ENST00000689011.1:c.300-226T=
ENST00000003084.11:c.3718-226T= MANE Select	ENSP00000003084.6:n.3718-226T=
ENST00000647720.1:c.1168-226T=
ENST00000649781.1:c.3535-226T=	ENSP00000497203.1:n.3535-226T=
ENST00000003084.10:c.3718-226T=	ENSP00000003084.6:n.3718-226T=
ENST00000426809.5:c.3628-226T=	ENSP00000389119.1:n.3628-226T=
NM_000492.3:c.3718-226T= , LRG_663t1:c.3718-226T=	NP_000483.3:n.3718-226T=
XM_011515751.1:c.3808-226T=	XP_011514053.1:n.3808-226T=
XM_011515752.1:c.3808-226T=	XP_011514054.1:n.3808-226T=
XM_011515753.1:c.3475-226T=	XP_011514055.1:n.3475-226T=
XM_011515754.1:c.3475-226T=	XP_011514056.1:n.3475-226T=
NM_000492.4:c.3718-226T= MANE Select	NP_000483.3:n.3718-226T=