Canonical Allele Identifier: CA2684621118

Gene: CFTR

Linked Data

• gnomAD v4: 7-117665661-AGTTCTTTTC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117665662_117665670del , CM000669.2:g.117665662_117665670del	GRCh38
NC_000007.13:g.117305716_117305724del , CM000669.1:g.117305716_117305724del	GRCh37
NC_000007.12:g.117092952_117092960del	NCBI36
NG_016465.4:g.204879_204887del , LRG_663:g.204879_204887del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.*451+98_*451+106del	ENSP00000497673.2:n.*451+98_*451+106del
ENST00000647978.2:c.*3956+98_*3956+106del	ENSP00000497658.1:n.*3956+98_*3956+106del
ENST00000649781.2:c.4059+98_4059+106del	ENSP00000497203.1:n.4059+98_4059+106del
ENST00000685018.2:c.*455+98_*455+106del	ENSP00000510194.2:n.*455+98_*455+106del
ENST00000687278.2:c.*895+98_*895+106del	ENSP00000509593.2:n.*895+98_*895+106del
ENST00000699585.1:c.*451+98_*451+106del	ENSP00000514456.1:n.*451+98_*451+106del
ENST00000699598.1:c.4242+98_4242+106del	ENSP00000514467.1:n.4242+98_4242+106del
ENST00000699599.1:c.*455+98_*455+106del	ENSP00000514468.1:n.*455+98_*455+106del
ENST00000699600.1:c.*903+98_*903+106del	ENSP00000514469.1:n.*903+98_*903+106del
ENST00000699601.1:c.*2617+98_*2617+106del	ENSP00000514470.1:n.*2617+98_*2617+106del
ENST00000699602.1:c.4236+98_4236+106del	ENSP00000514471.1:n.4236+98_4236+106del
ENST00000699604.1:c.*4066+98_*4066+106del	ENSP00000514472.1:n.*4066+98_*4066+106del
ENST00000699605.1:c.3816+98_3816+106del	ENSP00000514473.1:n.3816+98_3816+106del
ENST00000699606.1:n.2508_2516del
ENST00000685018.1:c.1106+98_1106+106del	ENSP00000510194.1:n.1106+98_1106+106del
ENST00000687278.1:c.2029+98_2029+106del	ENSP00000509593.1:n.2029+98_2029+106del
ENST00000689011.1:c.824+98_824+106del
ENST00000003084.11:c.4242+98_4242+106del MANE Select	ENSP00000003084.6:n.4242+98_4242+106del
ENST00000647720.1:c.1692+98_1692+106del
ENST00000649781.1:c.4059+98_4059+106del	ENSP00000497203.1:n.4059+98_4059+106del
ENST00000003084.10:c.4242+98_4242+106del	ENSP00000003084.6:n.4242+98_4242+106del
ENST00000426809.5:c.4152+98_4152+106del	ENSP00000389119.1:n.4152+98_4152+106del
ENST00000600166.1:c.368+98_368+106del
NM_000492.3:c.4242+98_4242+106del , LRG_663t1:c.4242+98_4242+106del	NP_000483.3:n.4242+98_4242+106del
XM_011515751.1:c.4332+98_4332+106del	XP_011514053.1:n.4332+98_4332+106del
XM_011515752.1:c.4332+98_4332+106del	XP_011514054.1:n.4332+98_4332+106del
XM_011515753.1:c.3999+98_3999+106del	XP_011514055.1:n.3999+98_3999+106del
XM_011515754.1:c.3999+98_3999+106del	XP_011514056.1:n.3999+98_3999+106del
NM_000492.4:c.4242+98_4242+106del MANE Select	NP_000483.3:n.4242+98_4242+106del