Canonical Allele Identifier: CA368983796

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117305608A>G (hg19) ; chr7:g.117665554A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117665554A>G , CM000669.2:g.117665554A>G	GRCh38
NC_000007.13:g.117305608A>G , CM000669.1:g.117305608A>G	GRCh37
NC_000007.12:g.117092844A>G	NCBI36
NG_016465.4:g.204771A>G , LRG_663:g.204771A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.*441A>G	ENSP00000497673.2:n.*441A>G
ENST00000647978.2:c.*3946A>G	ENSP00000497658.1:n.*3946A>G
ENST00000649781.2:c.4049A>G	ENSP00000497203.1:p.Gln1350Arg
ENST00000685018.2:c.*445A>G	ENSP00000510194.2:n.*445A>G
ENST00000687278.2:c.*885A>G	ENSP00000509593.2:n.*885A>G
ENST00000699585.1:c.*441A>G	ENSP00000514456.1:n.*441A>G
ENST00000699598.1:c.4232A>G	ENSP00000514467.1:p.Gln1411Arg
ENST00000699599.1:c.*445A>G	ENSP00000514468.1:n.*445A>G
ENST00000699600.1:c.*893A>G	ENSP00000514469.1:n.*893A>G
ENST00000699601.1:c.*2607A>G	ENSP00000514470.1:n.*2607A>G
ENST00000699602.1:c.4226A>G	ENSP00000514471.1:p.Gln1409Arg
ENST00000699604.1:c.*4056A>G	ENSP00000514472.1:n.*4056A>G
ENST00000699605.1:c.3806A>G	ENSP00000514473.1:p.Gln1269Arg
ENST00000699606.1:n.2400A>G
ENST00000685018.1:c.1096A>G	ENSP00000510194.1:n.1096A>G
ENST00000687278.1:c.2019A>G	ENSP00000509593.1:n.2019A>G
ENST00000689011.1:c.814A>G
ENST00000003084.11:c.4232A>G MANE Select	ENSP00000003084.6:p.Gln1411Arg
ENST00000647720.1:c.1682A>G
ENST00000649781.1:c.4049A>G	ENSP00000497203.1:p.Gln1350Arg
ENST00000003084.10:c.4232A>G	ENSP00000003084.6:p.Gln1411Arg
ENST00000426809.5:c.4142A>G	ENSP00000389119.1:p.Gln1381Arg
ENST00000600166.1:c.358A>G
NM_000492.3:c.4232A>G , LRG_663t1:c.4232A>G	NP_000483.3:p.Gln1411Arg
XM_011515751.1:c.4322A>G	XP_011514053.1:p.Gln1441Arg
XM_011515752.1:c.4322A>G	XP_011514054.1:p.Gln1441Arg
XM_011515753.1:c.3989A>G	XP_011514055.1:p.Gln1330Arg
XM_011515754.1:c.3989A>G	XP_011514056.1:p.Gln1330Arg
NM_000492.4:c.4232A>G MANE Select	NP_000483.3:p.Gln1411Arg