Canonical Allele Identifier: CA1737404733

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117642451G= , CM000669.2:g.117642451G=	GRCh38
NC_000007.13:g.117282505G= , CM000669.1:g.117282505G=	GRCh37
NC_000007.12:g.117069741G=	NCBI36
NG_016465.4:g.181668G= , LRG_663:g.181668G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000492.4:c.3731G= MANE Select	NP_000483.3:p.Gly1244=
ENST00000003084.11:c.3731G= MANE Select	ENSP00000003084.6:p.Gly1244=
NM_000492.3:c.3731G= , LRG_663t1:c.3731G=	NP_000483.3:p.Gly1244=
ENST00000003084.10:c.3731G=	ENSP00000003084.6:p.Gly1244=
ENST00000426809.5:c.3641G=	ENSP00000389119.1:p.Gly1214=
ENST00000647720.1:c.1181G=
ENST00000647720.2:c.3531G=	ENSP00000497673.2:p.Gly1177=
ENST00000647978.2:c.*3445G=	ENSP00000497658.1:n.*3445G=
ENST00000649781.1:c.3548G=	ENSP00000497203.1:p.Gly1183=
ENST00000649781.2:c.3548G=	ENSP00000497203.1:p.Gly1183=
ENST00000685018.1:c.479G=	ENSP00000510194.1:p.Gly160=
ENST00000685018.2:c.3731G=	ENSP00000510194.2:p.Gly1244=
ENST00000687278.1:c.1518G=	ENSP00000509593.1:n.1518G=
ENST00000687278.2:c.*384G=	ENSP00000509593.2:n.*384G=
ENST00000689011.1:c.313G=
ENST00000699585.1:c.3531G=	ENSP00000514456.1:p.Gly1177=
ENST00000699598.1:c.3731G=	ENSP00000514467.1:p.Gly1244=
ENST00000699599.1:c.3731G=	ENSP00000514468.1:p.Gly1244=
ENST00000699600.1:c.*392G=	ENSP00000514469.1:n.*392G=
ENST00000699601.1:c.*2106G=	ENSP00000514470.1:n.*2106G=
ENST00000699602.1:c.3725G=	ENSP00000514471.1:p.Gly1242=
ENST00000699604.1:c.*3555G=	ENSP00000514472.1:n.*3555G=
ENST00000699605.1:c.3305G=	ENSP00000514473.1:p.Gly1102=
XM_011515751.1:c.3821G=	XP_011514053.1:p.Gly1274=
XM_011515752.1:c.3821G=	XP_011514054.1:p.Gly1274=
XM_011515753.1:c.3488G=	XP_011514055.1:p.Gly1163=
XM_011515754.1:c.3488G=	XP_011514056.1:p.Gly1163=