Canonical Allele Identifier: CA326964

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117606674G>A , CM000669.2:g.117606674G>A	GRCh38
NC_000007.13:g.117246728G>A , CM000669.1:g.117246728G>A	GRCh37
NC_000007.12:g.117033964G>A	NCBI36
NG_016465.4:g.145891G>A , LRG_663:g.145891G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000492.4:c.2909G>A MANE Select	NP_000483.3:p.Gly970Asp
ENST00000003084.11:c.2909G>A MANE Select	ENSP00000003084.6:p.Gly970Asp
NM_000492.3:c.2909G>A , LRG_663t1:c.2909G>A	NP_000483.3:p.Gly970Asp
ENST00000003084.10:c.2909G>A	ENSP00000003084.6:p.Gly970Asp
ENST00000426809.5:c.2819G>A	ENSP00000389119.1:p.Gly940Asp
ENST00000647720.1:c.559G>A
ENST00000647720.2:c.2909G>A	ENSP00000497673.2:p.Gly970Asp
ENST00000647978.2:c.*2623G>A	ENSP00000497658.1:n.*2623G>A
ENST00000648260.1:c.1691G>A	ENSP00000497957.1:p.Gly564Asp
ENST00000649406.1:c.2726G>A	ENSP00000497965.1:p.Gly909Asp
ENST00000649781.1:c.2726G>A	ENSP00000497203.1:p.Gly909Asp
ENST00000649781.2:c.2726G>A	ENSP00000497203.1:p.Gly909Asp
ENST00000685018.2:c.2909G>A	ENSP00000510194.2:p.Gly970Asp
ENST00000687278.1:c.500G>A	ENSP00000509593.1:p.Gly167Asp
ENST00000687278.2:c.2909G>A	ENSP00000509593.2:p.Gly970Asp
ENST00000699585.1:c.2909G>A	ENSP00000514456.1:p.Gly970Asp
ENST00000699598.1:c.2909G>A	ENSP00000514467.1:p.Gly970Asp
ENST00000699599.1:c.2909G>A	ENSP00000514468.1:p.Gly970Asp
ENST00000699600.1:c.2909G>A	ENSP00000514469.1:p.Gly970Asp
ENST00000699601.1:c.*1209G>A	ENSP00000514470.1:n.*1209G>A
ENST00000699602.1:c.2909G>A	ENSP00000514471.1:p.Gly970Asp
ENST00000699604.1:c.*2733G>A	ENSP00000514472.1:n.*2733G>A
ENST00000699605.1:c.2483G>A	ENSP00000514473.1:p.Gly828Asp
XM_011515751.1:c.2999G>A	XP_011514053.1:p.Gly1000Asp
XM_011515752.1:c.2999G>A	XP_011514054.1:p.Gly1000Asp
XM_011515753.1:c.2666G>A	XP_011514055.1:p.Gly889Asp
XM_011515754.1:c.2666G>A	XP_011514056.1:p.Gly889Asp