Canonical Allele Identifier: CA1737387886

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611833C= , CM000669.2:g.117611833C=	GRCh38
NC_000007.13:g.117251887C= , CM000669.1:g.117251887C=	GRCh37
NC_000007.12:g.117039123C=	NCBI36
NG_016465.4:g.151050C= , LRG_663:g.151050C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3367+25C=	ENSP00000497673.2:n.3367+25C=
ENST00000647978.2:c.*3081+25C=	ENSP00000497658.1:n.*3081+25C=
ENST00000649781.2:c.3184+25C=	ENSP00000497203.1:n.3184+25C=
ENST00000685018.2:c.3367+25C=	ENSP00000510194.2:n.3367+25C=
ENST00000687278.2:c.3367+25C=	ENSP00000509593.2:n.3367+25C=
ENST00000699585.1:c.3367+25C=	ENSP00000514456.1:n.3367+25C=
ENST00000699598.1:c.3367+25C=	ENSP00000514467.1:n.3367+25C=
ENST00000699599.1:c.3367+25C=	ENSP00000514468.1:n.3367+25C=
ENST00000699600.1:c.3367+25C=	ENSP00000514469.1:n.3367+25C=
ENST00000699601.1:c.*1667+25C=	ENSP00000514470.1:n.*1667+25C=
ENST00000699602.1:c.3367+25C=	ENSP00000514471.1:n.3367+25C=
ENST00000699604.1:c.*3191+25C=	ENSP00000514472.1:n.*3191+25C=
ENST00000699605.1:c.2941+25C=	ENSP00000514473.1:n.2941+25C=
ENST00000685018.1:c.115+25C=	ENSP00000510194.1:n.115+25C=
ENST00000687278.1:c.958+25C=	ENSP00000509593.1:n.958+25C=
ENST00000003084.11:c.3367+25C= MANE Select	ENSP00000003084.6:n.3367+25C=
ENST00000647720.1:c.1017+25C=
ENST00000648260.1:c.2149+25C=	ENSP00000497957.1:n.2149+25C=
ENST00000649406.1:c.3184+25C=	ENSP00000497965.1:n.3184+25C=
ENST00000649781.1:c.3184+25C=	ENSP00000497203.1:n.3184+25C=
ENST00000003084.10:c.3367+25C=	ENSP00000003084.6:n.3367+25C=
ENST00000426809.5:c.3277+25C=	ENSP00000389119.1:n.3277+25C=
ENST00000468795.1:c.192+25C=
NM_000492.3:c.3367+25C= , LRG_663t1:c.3367+25C=	NP_000483.3:n.3367+25C=
XM_011515751.1:c.3457+25C=	XP_011514053.1:n.3457+25C=
XM_011515752.1:c.3457+25C=	XP_011514054.1:n.3457+25C=
XM_011515753.1:c.3124+25C=	XP_011514055.1:n.3124+25C=
XM_011515754.1:c.3124+25C=	XP_011514056.1:n.3124+25C=
NM_000492.4:c.3367+25C= MANE Select	NP_000483.3:n.3367+25C=