Canonical Allele Identifier: CA2684649267

Gene: CFTR

Linked Data

• gnomAD v4: 7-117665352-GAAAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117665355_117665358del , CM000669.2:g.117665355_117665358del	GRCh38
NC_000007.13:g.117305409_117305412del , CM000669.1:g.117305409_117305412del	GRCh37
NC_000007.12:g.117092645_117092648del	NCBI36
NG_016465.4:g.204572_204575del , LRG_663:g.204572_204575del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.*346-104_*346-101del	ENSP00000497673.2:n.*346-104_*346-101del
ENST00000647978.2:c.*3851-104_*3851-101del	ENSP00000497658.1:n.*3851-104_*3851-101de...
ENST00000649781.2:c.3954-104_3954-101del	ENSP00000497203.1:n.3954-104_3954-101del
ENST00000685018.2:c.*350-104_*350-101del	ENSP00000510194.2:n.*350-104_*350-101del
ENST00000687278.2:c.*790-104_*790-101del	ENSP00000509593.2:n.*790-104_*790-101del
ENST00000699585.1:c.*346-104_*346-101del	ENSP00000514456.1:n.*346-104_*346-101del
ENST00000699598.1:c.4137-104_4137-101del	ENSP00000514467.1:n.4137-104_4137-101del
ENST00000699599.1:c.*350-104_*350-101del	ENSP00000514468.1:n.*350-104_*350-101del
ENST00000699600.1:c.*798-104_*798-101del	ENSP00000514469.1:n.*798-104_*798-101del
ENST00000699601.1:c.*2512-104_*2512-101del	ENSP00000514470.1:n.*2512-104_*2512-101de...
ENST00000699602.1:c.4131-104_4131-101del	ENSP00000514471.1:n.4131-104_4131-101del
ENST00000699604.1:c.*3961-104_*3961-101del	ENSP00000514472.1:n.*3961-104_*3961-101de...
ENST00000699605.1:c.3711-104_3711-101del	ENSP00000514473.1:n.3711-104_3711-101del
ENST00000699606.1:n.2305-104_2305-101del
ENST00000685018.1:c.1001-104_1001-101del	ENSP00000510194.1:n.1001-104_1001-101del
ENST00000687278.1:c.1924-104_1924-101del	ENSP00000509593.1:n.1924-104_1924-101del
ENST00000689011.1:c.719-104_719-101del
ENST00000003084.11:c.4137-104_4137-101del MANE Select	ENSP00000003084.6:n.4137-104_4137-101del
ENST00000647720.1:c.1587-104_1587-101del
ENST00000649781.1:c.3954-104_3954-101del	ENSP00000497203.1:n.3954-104_3954-101del
ENST00000003084.10:c.4137-104_4137-101del	ENSP00000003084.6:n.4137-104_4137-101del
ENST00000426809.5:c.4047-104_4047-101del	ENSP00000389119.1:n.4047-104_4047-101del
ENST00000600166.1:c.263-104_263-101del
NM_000492.3:c.4137-104_4137-101del , LRG_663t1:c.4137-104_4137-101del	NP_000483.3:n.4137-104_4137-101del
XM_011515751.1:c.4227-104_4227-101del	XP_011514053.1:n.4227-104_4227-101del
XM_011515752.1:c.4227-104_4227-101del	XP_011514054.1:n.4227-104_4227-101del
XM_011515753.1:c.3894-104_3894-101del	XP_011514055.1:n.3894-104_3894-101del
XM_011515754.1:c.3894-104_3894-101del	XP_011514056.1:n.3894-104_3894-101del
NM_000492.4:c.4137-104_4137-101del MANE Select	NP_000483.3:n.4137-104_4137-101del