Canonical Allele Identifier: CA1737374900

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603638G= , CM000669.2:g.117603638G=	GRCh38
NC_000007.13:g.117243692G= , CM000669.1:g.117243692G=	GRCh37
NC_000007.12:g.117030928G=	NCBI36
NG_016465.4:g.142855G= , LRG_663:g.142855G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2764G=	ENSP00000497673.2:p.Val922=
ENST00000647978.2:c.*2478G=	ENSP00000497658.1:n.*2478G=
ENST00000649781.2:c.2581G=	ENSP00000497203.1:p.Val861=
ENST00000685018.2:c.2764G=	ENSP00000510194.2:p.Val922=
ENST00000687278.2:c.2764G=	ENSP00000509593.2:p.Val922=
ENST00000699585.1:c.2764G=	ENSP00000514456.1:p.Val922=
ENST00000699598.1:c.2764G=	ENSP00000514467.1:p.Val922=
ENST00000699599.1:c.2764G=	ENSP00000514468.1:p.Val922=
ENST00000699600.1:c.2764G=	ENSP00000514469.1:p.Val922=
ENST00000699601.1:c.*1064G=	ENSP00000514470.1:n.*1064G=
ENST00000699602.1:c.2764G=	ENSP00000514471.1:p.Val922=
ENST00000699604.1:c.*2588G=	ENSP00000514472.1:n.*2588G=
ENST00000699605.1:c.2338G=	ENSP00000514473.1:p.Val780=
ENST00000687278.1:c.355G=	ENSP00000509593.1:p.Val119=
ENST00000003084.11:c.2764G= MANE Select	ENSP00000003084.6:p.Val922=
ENST00000647720.1:c.414G=
ENST00000648260.1:c.1546G=	ENSP00000497957.1:p.Val516=
ENST00000649406.1:c.2581G=	ENSP00000497965.1:p.Val861=
ENST00000649781.1:c.2581G=	ENSP00000497203.1:p.Val861=
ENST00000003084.10:c.2764G=	ENSP00000003084.6:p.Val922=
ENST00000426809.5:c.2674G=	ENSP00000389119.1:p.Val892=
NM_000492.3:c.2764G= , LRG_663t1:c.2764G=	NP_000483.3:p.Val922=
XM_011515751.1:c.2854G=	XP_011514053.1:p.Val952=
XM_011515752.1:c.2854G=	XP_011514054.1:p.Val952=
XM_011515753.1:c.2521G=	XP_011514055.1:p.Val841=
XM_011515754.1:c.2521G=	XP_011514056.1:p.Val841=
NM_000492.4:c.2764G= MANE Select	NP_000483.3:p.Val922=