Canonical Allele Identifier: CA1737392104

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117614662_117614665delinsCATG , CM000669.2:g.117614662_117614665delinsCATG	GRCh38
NC_000007.13:g.117254716_117254719delinsCATG , CM000669.1:g.117254716_117254719delinsCATG	GRCh37
NC_000007.12:g.117041952_117041955delinsCATG	NCBI36
NG_016465.4:g.153879_153882delinsCATG , LRG_663:g.153879_153882delinsCATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3417_3420delinsCATG	ENSP00000497673.2:p.Ile1139=
ENST00000647978.2:c.*3131_*3134delinsCATG	ENSP00000497658.1:n.*3131_*3134delinsCATG
ENST00000649781.2:c.3234_3237delinsCATG	ENSP00000497203.1:p.Ile1078=
ENST00000685018.2:c.3417_3420delinsCATG	ENSP00000510194.2:p.Ile1139=
ENST00000687278.2:c.3417_3420delinsCATG	ENSP00000509593.2:p.Ile1139=
ENST00000699585.1:c.3417_3420delinsCATG	ENSP00000514456.1:p.Ile1139=
ENST00000699598.1:c.3417_3420delinsCATG	ENSP00000514467.1:p.Ile1139=
ENST00000699599.1:c.3417_3420delinsCATG	ENSP00000514468.1:p.Ile1139=
ENST00000699600.1:c.3417_3420delinsCATG	ENSP00000514469.1:p.Ile1139=
ENST00000699601.1:c.*1792_*1795delinsCATG	ENSP00000514470.1:n.*1792_*1795delinsCATG
ENST00000699602.1:c.3411_3414delinsCATG	ENSP00000514471.1:p.Ile1137=
ENST00000699604.1:c.*3241_*3244delinsCATG	ENSP00000514472.1:n.*3241_*3244delinsCATG
ENST00000699605.1:c.2991_2994delinsCATG	ENSP00000514473.1:p.Ile997=
ENST00000685018.1:c.165_168delinsCATG	ENSP00000510194.1:p.Ile55=
ENST00000687278.1:c.1008_1011delinsCATG	ENSP00000509593.1:p.Ile336=
ENST00000003084.11:c.3417_3420delinsCATG MANE Select	ENSP00000003084.6:p.Ile1139=
ENST00000647720.1:c.1067_1070delinsCATG
ENST00000648260.1:c.2199_2202delinsCATG	ENSP00000497957.1:p.Ile733=
ENST00000649406.1:c.3234_3237delinsCATG	ENSP00000497965.1:p.Ile1078=
ENST00000649781.1:c.3234_3237delinsCATG	ENSP00000497203.1:p.Ile1078=
ENST00000003084.10:c.3417_3420delinsCATG	ENSP00000003084.6:p.Ile1139=
ENST00000426809.5:c.3327_3330delinsCATG	ENSP00000389119.1:p.Ile1109=
ENST00000468795.1:c.242_245delinsCATG
NM_000492.3:c.3417_3420delinsCATG , LRG_663t1:c.3417_3420delinsCATG	NP_000483.3:p.Ile1139=
XM_011515751.1:c.3507_3510delinsCATG	XP_011514053.1:p.Ile1169=
XM_011515752.1:c.3507_3510delinsCATG	XP_011514054.1:p.Ile1169=
XM_011515753.1:c.3174_3177delinsCATG	XP_011514055.1:p.Ile1058=
XM_011515754.1:c.3174_3177delinsCATG	XP_011514056.1:p.Ile1058=
NM_000492.4:c.3417_3420delinsCATG MANE Select	NP_000483.3:p.Ile1139=