Canonical Allele Identifier: CA1737422911

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117665519_117665521delinsCTG , CM000669.2:g.117665519_117665521delinsCTG	GRCh38
NC_000007.13:g.117305573_117305575delinsCTG , CM000669.1:g.117305573_117305575delinsCTG	GRCh37
NC_000007.12:g.117092809_117092811delinsCTG	NCBI36
NG_016465.4:g.204736_204738delinsCTG , LRG_663:g.204736_204738delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.*406_*408delinsCTG	ENSP00000497673.2:n.*406_*408delinsCTG
ENST00000647978.2:c.*3911_*3913delinsCTG	ENSP00000497658.1:n.*3911_*3913delinsCTG
ENST00000649781.2:c.4014_4016delinsCTG	ENSP00000497203.1:p.Leu1338=
ENST00000685018.2:c.*410_*412delinsCTG	ENSP00000510194.2:n.*410_*412delinsCTG
ENST00000687278.2:c.*850_*852delinsCTG	ENSP00000509593.2:n.*850_*852delinsCTG
ENST00000699585.1:c.*406_*408delinsCTG	ENSP00000514456.1:n.*406_*408delinsCTG
ENST00000699598.1:c.4197_4199delinsCTG	ENSP00000514467.1:p.Leu1399=
ENST00000699599.1:c.*410_*412delinsCTG	ENSP00000514468.1:n.*410_*412delinsCTG
ENST00000699600.1:c.*858_*860delinsCTG	ENSP00000514469.1:n.*858_*860delinsCTG
ENST00000699601.1:c.*2572_*2574delinsCTG	ENSP00000514470.1:n.*2572_*2574delinsCTG
ENST00000699602.1:c.4191_4193delinsCTG	ENSP00000514471.1:p.Leu1397=
ENST00000699604.1:c.*4021_*4023delinsCTG	ENSP00000514472.1:n.*4021_*4023delinsCTG
ENST00000699605.1:c.3771_3773delinsCTG	ENSP00000514473.1:p.Leu1257=
ENST00000699606.1:n.2365_2367delinsCTG
ENST00000685018.1:c.1061_1063delinsCTG	ENSP00000510194.1:n.1061_1063delinsCTG
ENST00000687278.1:c.1984_1986delinsCTG	ENSP00000509593.1:n.1984_1986delinsCTG
ENST00000689011.1:c.779_781delinsCTG
ENST00000003084.11:c.4197_4199delinsCTG MANE Select	ENSP00000003084.6:p.Leu1399=
ENST00000647720.1:c.1647_1649delinsCTG
ENST00000649781.1:c.4014_4016delinsCTG	ENSP00000497203.1:p.Leu1338=
ENST00000003084.10:c.4197_4199delinsCTG	ENSP00000003084.6:p.Leu1399=
ENST00000426809.5:c.4107_4109delinsCTG	ENSP00000389119.1:p.Leu1369=
ENST00000600166.1:c.323_325delinsCTG
NM_000492.3:c.4197_4199delinsCTG , LRG_663t1:c.4197_4199delinsCTG	NP_000483.3:p.Leu1399=
XM_011515751.1:c.4287_4289delinsCTG	XP_011514053.1:p.Leu1429=
XM_011515752.1:c.4287_4289delinsCTG	XP_011514054.1:p.Leu1429=
XM_011515753.1:c.3954_3956delinsCTG	XP_011514055.1:p.Leu1318=
XM_011515754.1:c.3954_3956delinsCTG	XP_011514056.1:p.Leu1318=
NM_000492.4:c.4197_4199delinsCTG MANE Select	NP_000483.3:p.Leu1399=