Canonical Allele Identifier: CA2684621092

Gene: CFTR

Linked Data

• gnomAD v4: 7-117665618-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117665619_117665620del , CM000669.2:g.117665619_117665620del	GRCh38
NC_000007.13:g.117305673_117305674del , CM000669.1:g.117305673_117305674del	GRCh37
NC_000007.12:g.117092909_117092910del	NCBI36
NG_016465.4:g.204836_204837del , LRG_663:g.204836_204837del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.*451+55_*451+56del	ENSP00000497673.2:n.*451+55_*451+56del
ENST00000647978.2:c.*3956+55_*3956+56del	ENSP00000497658.1:n.*3956+55_*3956+56del
ENST00000649781.2:c.4059+55_4059+56del	ENSP00000497203.1:n.4059+55_4059+56del
ENST00000685018.2:c.*455+55_*455+56del	ENSP00000510194.2:n.*455+55_*455+56del
ENST00000687278.2:c.*895+55_*895+56del	ENSP00000509593.2:n.*895+55_*895+56del
ENST00000699585.1:c.*451+55_*451+56del	ENSP00000514456.1:n.*451+55_*451+56del
ENST00000699598.1:c.4242+55_4242+56del	ENSP00000514467.1:n.4242+55_4242+56del
ENST00000699599.1:c.*455+55_*455+56del	ENSP00000514468.1:n.*455+55_*455+56del
ENST00000699600.1:c.*903+55_*903+56del	ENSP00000514469.1:n.*903+55_*903+56del
ENST00000699601.1:c.*2617+55_*2617+56del	ENSP00000514470.1:n.*2617+55_*2617+56del
ENST00000699602.1:c.4236+55_4236+56del	ENSP00000514471.1:n.4236+55_4236+56del
ENST00000699604.1:c.*4066+55_*4066+56del	ENSP00000514472.1:n.*4066+55_*4066+56del
ENST00000699605.1:c.3816+55_3816+56del	ENSP00000514473.1:n.3816+55_3816+56del
ENST00000699606.1:n.2465_2466del
ENST00000685018.1:c.1106+55_1106+56del	ENSP00000510194.1:n.1106+55_1106+56del
ENST00000687278.1:c.2029+55_2029+56del	ENSP00000509593.1:n.2029+55_2029+56del
ENST00000689011.1:c.824+55_824+56del
ENST00000003084.11:c.4242+55_4242+56del MANE Select	ENSP00000003084.6:n.4242+55_4242+56del
ENST00000647720.1:c.1692+55_1692+56del
ENST00000649781.1:c.4059+55_4059+56del	ENSP00000497203.1:n.4059+55_4059+56del
ENST00000003084.10:c.4242+55_4242+56del	ENSP00000003084.6:n.4242+55_4242+56del
ENST00000426809.5:c.4152+55_4152+56del	ENSP00000389119.1:n.4152+55_4152+56del
ENST00000600166.1:c.368+55_368+56del
NM_000492.3:c.4242+55_4242+56del , LRG_663t1:c.4242+55_4242+56del	NP_000483.3:n.4242+55_4242+56del
XM_011515751.1:c.4332+55_4332+56del	XP_011514053.1:n.4332+55_4332+56del
XM_011515752.1:c.4332+55_4332+56del	XP_011514054.1:n.4332+55_4332+56del
XM_011515753.1:c.3999+55_3999+56del	XP_011514055.1:n.3999+55_3999+56del
XM_011515754.1:c.3999+55_3999+56del	XP_011514056.1:n.3999+55_3999+56del
NM_000492.4:c.4242+55_4242+56del MANE Select	NP_000483.3:n.4242+55_4242+56del