Canonical Allele Identifier: CA1737404760

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117642491T= , CM000669.2:g.117642491T=	GRCh38
NC_000007.13:g.117282545T= , CM000669.1:g.117282545T=	GRCh37
NC_000007.12:g.117069781T=	NCBI36
NG_016465.4:g.181708T= , LRG_663:g.181708T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3571T=	ENSP00000497673.2:p.Phe1191=
ENST00000647978.2:c.*3485T=	ENSP00000497658.1:n.*3485T=
ENST00000649781.2:c.3588T=	ENSP00000497203.1:p.Phe1196=
ENST00000685018.2:c.3771T=	ENSP00000510194.2:p.Phe1257=
ENST00000687278.2:c.*424T=	ENSP00000509593.2:n.*424T=
ENST00000699585.1:c.3571T=	ENSP00000514456.1:p.Phe1191=
ENST00000699598.1:c.3771T=	ENSP00000514467.1:p.Phe1257=
ENST00000699599.1:c.3771T=	ENSP00000514468.1:p.Phe1257=
ENST00000699600.1:c.*432T=	ENSP00000514469.1:n.*432T=
ENST00000699601.1:c.*2146T=	ENSP00000514470.1:n.*2146T=
ENST00000699602.1:c.3765T=	ENSP00000514471.1:p.Phe1255=
ENST00000699604.1:c.*3595T=	ENSP00000514472.1:n.*3595T=
ENST00000699605.1:c.3345T=	ENSP00000514473.1:p.Phe1115=
ENST00000685018.1:c.519T=	ENSP00000510194.1:p.Phe173=
ENST00000687278.1:c.1558T=	ENSP00000509593.1:n.1558T=
ENST00000689011.1:c.353T=
ENST00000003084.11:c.3771T= MANE Select	ENSP00000003084.6:p.Phe1257=
ENST00000647720.1:c.1221T=
ENST00000649781.1:c.3588T=	ENSP00000497203.1:p.Phe1196=
ENST00000003084.10:c.3771T=	ENSP00000003084.6:p.Phe1257=
ENST00000426809.5:c.3681T=	ENSP00000389119.1:p.Phe1227=
NM_000492.3:c.3771T= , LRG_663t1:c.3771T=	NP_000483.3:p.Phe1257=
XM_011515751.1:c.3861T=	XP_011514053.1:p.Phe1287=
XM_011515752.1:c.3861T=	XP_011514054.1:p.Phe1287=
XM_011515753.1:c.3528T=	XP_011514055.1:p.Phe1176=
XM_011515754.1:c.3528T=	XP_011514056.1:p.Phe1176=
NM_000492.4:c.3771T= MANE Select	NP_000483.3:p.Phe1257=