Canonical Allele Identifier: CA2684621097

Gene: CFTR

Linked Data

• gnomAD v4: 7-117665626-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117665627_117665628del , CM000669.2:g.117665627_117665628del	GRCh38
NC_000007.13:g.117305681_117305682del , CM000669.1:g.117305681_117305682del	GRCh37
NC_000007.12:g.117092917_117092918del	NCBI36
NG_016465.4:g.204844_204845del , LRG_663:g.204844_204845del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.*451+63_*451+64del	ENSP00000497673.2:n.*451+63_*451+64del
ENST00000647978.2:c.*3956+63_*3956+64del	ENSP00000497658.1:n.*3956+63_*3956+64del
ENST00000649781.2:c.4059+63_4059+64del	ENSP00000497203.1:n.4059+63_4059+64del
ENST00000685018.2:c.*455+63_*455+64del	ENSP00000510194.2:n.*455+63_*455+64del
ENST00000687278.2:c.*895+63_*895+64del	ENSP00000509593.2:n.*895+63_*895+64del
ENST00000699585.1:c.*451+63_*451+64del	ENSP00000514456.1:n.*451+63_*451+64del
ENST00000699598.1:c.4242+63_4242+64del	ENSP00000514467.1:n.4242+63_4242+64del
ENST00000699599.1:c.*455+63_*455+64del	ENSP00000514468.1:n.*455+63_*455+64del
ENST00000699600.1:c.*903+63_*903+64del	ENSP00000514469.1:n.*903+63_*903+64del
ENST00000699601.1:c.*2617+63_*2617+64del	ENSP00000514470.1:n.*2617+63_*2617+64del
ENST00000699602.1:c.4236+63_4236+64del	ENSP00000514471.1:n.4236+63_4236+64del
ENST00000699604.1:c.*4066+63_*4066+64del	ENSP00000514472.1:n.*4066+63_*4066+64del
ENST00000699605.1:c.3816+63_3816+64del	ENSP00000514473.1:n.3816+63_3816+64del
ENST00000699606.1:n.2473_2474del
ENST00000685018.1:c.1106+63_1106+64del	ENSP00000510194.1:n.1106+63_1106+64del
ENST00000687278.1:c.2029+63_2029+64del	ENSP00000509593.1:n.2029+63_2029+64del
ENST00000689011.1:c.824+63_824+64del
ENST00000003084.11:c.4242+63_4242+64del MANE Select	ENSP00000003084.6:n.4242+63_4242+64del
ENST00000647720.1:c.1692+63_1692+64del
ENST00000649781.1:c.4059+63_4059+64del	ENSP00000497203.1:n.4059+63_4059+64del
ENST00000003084.10:c.4242+63_4242+64del	ENSP00000003084.6:n.4242+63_4242+64del
ENST00000426809.5:c.4152+63_4152+64del	ENSP00000389119.1:n.4152+63_4152+64del
ENST00000600166.1:c.368+63_368+64del
NM_000492.3:c.4242+63_4242+64del , LRG_663t1:c.4242+63_4242+64del	NP_000483.3:n.4242+63_4242+64del
XM_011515751.1:c.4332+63_4332+64del	XP_011514053.1:n.4332+63_4332+64del
XM_011515752.1:c.4332+63_4332+64del	XP_011514054.1:n.4332+63_4332+64del
XM_011515753.1:c.3999+63_3999+64del	XP_011514055.1:n.3999+63_3999+64del
XM_011515754.1:c.3999+63_3999+64del	XP_011514056.1:n.3999+63_3999+64del
NM_000492.4:c.4242+63_4242+64del MANE Select	NP_000483.3:n.4242+63_4242+64del