Canonical Allele Identifier: CA368983738

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117305591A>T (hg19) ; chr7:g.117665537A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117665537A>T , CM000669.2:g.117665537A>T	GRCh38
NC_000007.13:g.117305591A>T , CM000669.1:g.117305591A>T	GRCh37
NC_000007.12:g.117092827A>T	NCBI36
NG_016465.4:g.204754A>T , LRG_663:g.204754A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.*424A>T	ENSP00000497673.2:n.*424A>T
ENST00000647978.2:c.*3929A>T	ENSP00000497658.1:n.*3929A>T
ENST00000649781.2:c.4032A>T	ENSP00000497203.1:p.Glu1344Asp
ENST00000685018.2:c.*428A>T	ENSP00000510194.2:n.*428A>T
ENST00000687278.2:c.*868A>T	ENSP00000509593.2:n.*868A>T
ENST00000699585.1:c.*424A>T	ENSP00000514456.1:n.*424A>T
ENST00000699598.1:c.4215A>T	ENSP00000514467.1:p.Glu1405Asp
ENST00000699599.1:c.*428A>T	ENSP00000514468.1:n.*428A>T
ENST00000699600.1:c.*876A>T	ENSP00000514469.1:n.*876A>T
ENST00000699601.1:c.*2590A>T	ENSP00000514470.1:n.*2590A>T
ENST00000699602.1:c.4209A>T	ENSP00000514471.1:p.Glu1403Asp
ENST00000699604.1:c.*4039A>T	ENSP00000514472.1:n.*4039A>T
ENST00000699605.1:c.3789A>T	ENSP00000514473.1:p.Glu1263Asp
ENST00000699606.1:n.2383A>T
ENST00000685018.1:c.1079A>T	ENSP00000510194.1:n.1079A>T
ENST00000687278.1:c.2002A>T	ENSP00000509593.1:n.2002A>T
ENST00000689011.1:c.797A>T
ENST00000003084.11:c.4215A>T MANE Select	ENSP00000003084.6:p.Glu1405Asp
ENST00000647720.1:c.1665A>T
ENST00000649781.1:c.4032A>T	ENSP00000497203.1:p.Glu1344Asp
ENST00000003084.10:c.4215A>T	ENSP00000003084.6:p.Glu1405Asp
ENST00000426809.5:c.4125A>T	ENSP00000389119.1:p.Glu1375Asp
ENST00000600166.1:c.341A>T
NM_000492.3:c.4215A>T , LRG_663t1:c.4215A>T	NP_000483.3:p.Glu1405Asp
XM_011515751.1:c.4305A>T	XP_011514053.1:p.Glu1435Asp
XM_011515752.1:c.4305A>T	XP_011514054.1:p.Glu1435Asp
XM_011515753.1:c.3972A>T	XP_011514055.1:p.Glu1324Asp
XM_011515754.1:c.3972A>T	XP_011514056.1:p.Glu1324Asp
NM_000492.4:c.4215A>T MANE Select	NP_000483.3:p.Glu1405Asp