Canonical Allele Identifier: CA1737404668

Gene: CFTR

Linked Data

• dbSNP Id: rs1792928099
• gnomAD v4: 7-117642289-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117642289G>A , CM000669.2:g.117642289G>A	GRCh38
NC_000007.13:g.117282343G>A , CM000669.1:g.117282343G>A	GRCh37
NC_000007.12:g.117069579G>A	NCBI36
NG_016465.4:g.181506G>A , LRG_663:g.181506G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3518-149G>A	ENSP00000497673.2:n.3518-149G>A
ENST00000647978.2:c.*3432-149G>A	ENSP00000497658.1:n.*3432-149G>A
ENST00000649781.2:c.3535-149G>A	ENSP00000497203.1:n.3535-149G>A
ENST00000685018.2:c.3718-149G>A	ENSP00000510194.2:n.3718-149G>A
ENST00000687278.2:c.*371-149G>A	ENSP00000509593.2:n.*371-149G>A
ENST00000699585.1:c.3518-149G>A	ENSP00000514456.1:n.3518-149G>A
ENST00000699598.1:c.3718-149G>A	ENSP00000514467.1:n.3718-149G>A
ENST00000699599.1:c.3718-149G>A	ENSP00000514468.1:n.3718-149G>A
ENST00000699600.1:c.*379-149G>A	ENSP00000514469.1:n.*379-149G>A
ENST00000699601.1:c.*2093-149G>A	ENSP00000514470.1:n.*2093-149G>A
ENST00000699602.1:c.3712-149G>A	ENSP00000514471.1:n.3712-149G>A
ENST00000699604.1:c.*3542-149G>A	ENSP00000514472.1:n.*3542-149G>A
ENST00000699605.1:c.3292-149G>A	ENSP00000514473.1:n.3292-149G>A
ENST00000685018.1:c.466-149G>A	ENSP00000510194.1:n.466-149G>A
ENST00000687278.1:c.1505-149G>A	ENSP00000509593.1:n.1505-149G>A
ENST00000689011.1:c.300-149G>A
ENST00000003084.11:c.3718-149G>A MANE Select	ENSP00000003084.6:n.3718-149G>A
ENST00000647720.1:c.1168-149G>A
ENST00000649781.1:c.3535-149G>A	ENSP00000497203.1:n.3535-149G>A
ENST00000003084.10:c.3718-149G>A	ENSP00000003084.6:n.3718-149G>A
ENST00000426809.5:c.3628-149G>A	ENSP00000389119.1:n.3628-149G>A
NM_000492.3:c.3718-149G>A , LRG_663t1:c.3718-149G>A	NP_000483.3:n.3718-149G>A
XM_011515751.1:c.3808-149G>A	XP_011514053.1:n.3808-149G>A
XM_011515752.1:c.3808-149G>A	XP_011514054.1:n.3808-149G>A
XM_011515753.1:c.3475-149G>A	XP_011514055.1:n.3475-149G>A
XM_011515754.1:c.3475-149G>A	XP_011514056.1:n.3475-149G>A
NM_000492.4:c.3718-149G>A MANE Select	NP_000483.3:n.3718-149G>A