Canonical Allele Identifier: CA1737375395

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603730G= , CM000669.2:g.117603730G=	GRCh38
NC_000007.13:g.117243784G= , CM000669.1:g.117243784G=	GRCh37
NC_000007.12:g.117031020G=	NCBI36
NG_016465.4:g.142947G= , LRG_663:g.142947G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.2856G=	ENSP00000497673.2:p.Met952=
ENST00000647978.2:c.*2570G=	ENSP00000497658.1:n.*2570G=
ENST00000649781.2:c.2673G=	ENSP00000497203.1:p.Met891=
ENST00000685018.2:c.2856G=	ENSP00000510194.2:p.Met952=
ENST00000687278.2:c.2856G=	ENSP00000509593.2:p.Met952=
ENST00000699585.1:c.2856G=	ENSP00000514456.1:p.Met952=
ENST00000699598.1:c.2856G=	ENSP00000514467.1:p.Met952=
ENST00000699599.1:c.2856G=	ENSP00000514468.1:p.Met952=
ENST00000699600.1:c.2856G=	ENSP00000514469.1:p.Met952=
ENST00000699601.1:c.*1156G=	ENSP00000514470.1:n.*1156G=
ENST00000699602.1:c.2856G=	ENSP00000514471.1:p.Met952=
ENST00000699604.1:c.*2680G=	ENSP00000514472.1:n.*2680G=
ENST00000699605.1:c.2430G=	ENSP00000514473.1:p.Met810=
ENST00000687278.1:c.447G=	ENSP00000509593.1:p.Met149=
ENST00000003084.11:c.2856G= MANE Select	ENSP00000003084.6:p.Met952=
ENST00000647720.1:c.506G=
ENST00000648260.1:c.1638G=	ENSP00000497957.1:p.Met546=
ENST00000649406.1:c.2673G=	ENSP00000497965.1:p.Met891=
ENST00000649781.1:c.2673G=	ENSP00000497203.1:p.Met891=
ENST00000003084.10:c.2856G=	ENSP00000003084.6:p.Met952=
ENST00000426809.5:c.2766G=	ENSP00000389119.1:p.Met922=
NM_000492.3:c.2856G= , LRG_663t1:c.2856G=	NP_000483.3:p.Met952=
XM_011515751.1:c.2946G=	XP_011514053.1:p.Met982=
XM_011515752.1:c.2946G=	XP_011514054.1:p.Met982=
XM_011515753.1:c.2613G=	XP_011514055.1:p.Met871=
XM_011515754.1:c.2613G=	XP_011514056.1:p.Met871=
NM_000492.4:c.2856G= MANE Select	NP_000483.3:p.Met952=