Canonical Allele Identifier: CA1737423114

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117665594_117665595delinsCA , CM000669.2:g.117665594_117665595delinsCA	GRCh38
NC_000007.13:g.117305648_117305649delinsCA , CM000669.1:g.117305648_117305649delinsCA	GRCh37
NC_000007.12:g.117092884_117092885delinsCA	NCBI36
NG_016465.4:g.204811_204812delinsCA , LRG_663:g.204811_204812delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.*451+30_*451+31delinsCA	ENSP00000497673.2:n.*451+30_*451+31delinsCA
ENST00000647978.2:c.*3956+30_*3956+31delinsCA	ENSP00000497658.1:n.*3956+30_*3956+31delinsCA
ENST00000649781.2:c.4059+30_4059+31delinsCA	ENSP00000497203.1:n.4059+30_4059+31delinsCA
ENST00000685018.2:c.*455+30_*455+31delinsCA	ENSP00000510194.2:n.*455+30_*455+31delinsCA
ENST00000687278.2:c.*895+30_*895+31delinsCA	ENSP00000509593.2:n.*895+30_*895+31delinsCA
ENST00000699585.1:c.*451+30_*451+31delinsCA	ENSP00000514456.1:n.*451+30_*451+31delinsCA
ENST00000699598.1:c.4242+30_4242+31delinsCA	ENSP00000514467.1:n.4242+30_4242+31delinsCA
ENST00000699599.1:c.*455+30_*455+31delinsCA	ENSP00000514468.1:n.*455+30_*455+31delinsCA
ENST00000699600.1:c.*903+30_*903+31delinsCA	ENSP00000514469.1:n.*903+30_*903+31delinsCA
ENST00000699601.1:c.*2617+30_*2617+31delinsCA	ENSP00000514470.1:n.*2617+30_*2617+31delinsCA
ENST00000699602.1:c.4236+30_4236+31delinsCA	ENSP00000514471.1:n.4236+30_4236+31delinsCA
ENST00000699604.1:c.*4066+30_*4066+31delinsCA	ENSP00000514472.1:n.*4066+30_*4066+31delinsCA
ENST00000699605.1:c.3816+30_3816+31delinsCA	ENSP00000514473.1:n.3816+30_3816+31delinsCA
ENST00000699606.1:n.2440_2441delinsCA
ENST00000685018.1:c.1106+30_1106+31delinsCA	ENSP00000510194.1:n.1106+30_1106+31delinsCA
ENST00000687278.1:c.2029+30_2029+31delinsCA	ENSP00000509593.1:n.2029+30_2029+31delinsCA
ENST00000689011.1:c.824+30_824+31delinsCA
ENST00000003084.11:c.4242+30_4242+31delinsCA MANE Select	ENSP00000003084.6:n.4242+30_4242+31delinsCA
ENST00000647720.1:c.1692+30_1692+31delinsCA
ENST00000649781.1:c.4059+30_4059+31delinsCA	ENSP00000497203.1:n.4059+30_4059+31delinsCA
ENST00000003084.10:c.4242+30_4242+31delinsCA	ENSP00000003084.6:n.4242+30_4242+31delinsCA
ENST00000426809.5:c.4152+30_4152+31delinsCA	ENSP00000389119.1:n.4152+30_4152+31delinsCA
ENST00000600166.1:c.368+30_368+31delinsCA
NM_000492.3:c.4242+30_4242+31delinsCA , LRG_663t1:c.4242+30_4242+31delinsCA	NP_000483.3:n.4242+30_4242+31delinsCA
XM_011515751.1:c.4332+30_4332+31delinsCA	XP_011514053.1:n.4332+30_4332+31delinsCA
XM_011515752.1:c.4332+30_4332+31delinsCA	XP_011514054.1:n.4332+30_4332+31delinsCA
XM_011515753.1:c.3999+30_3999+31delinsCA	XP_011514055.1:n.3999+30_3999+31delinsCA
XM_011515754.1:c.3999+30_3999+31delinsCA	XP_011514056.1:n.3999+30_3999+31delinsCA
NM_000492.4:c.4242+30_4242+31delinsCA MANE Select	NP_000483.3:n.4242+30_4242+31delinsCA