Canonical Allele Identifier: CA1737386722

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611601C= , CM000669.2:g.117611601C=	GRCh38
NC_000007.13:g.117251655C= , CM000669.1:g.117251655C=	GRCh37
NC_000007.12:g.117038891C=	NCBI36
NG_016465.4:g.150818C= , LRG_663:g.150818C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3160C=	ENSP00000497673.2:p.His1054=
ENST00000647978.2:c.*2874C=	ENSP00000497658.1:n.*2874C=
ENST00000649781.2:c.2977C=	ENSP00000497203.1:p.His993=
ENST00000685018.2:c.3160C=	ENSP00000510194.2:p.His1054=
ENST00000687278.2:c.3160C=	ENSP00000509593.2:p.His1054=
ENST00000699585.1:c.3160C=	ENSP00000514456.1:p.His1054=
ENST00000699598.1:c.3160C=	ENSP00000514467.1:p.His1054=
ENST00000699599.1:c.3160C=	ENSP00000514468.1:p.His1054=
ENST00000699600.1:c.3160C=	ENSP00000514469.1:p.His1054=
ENST00000699601.1:c.*1460C=	ENSP00000514470.1:n.*1460C=
ENST00000699602.1:c.3160C=	ENSP00000514471.1:p.His1054=
ENST00000699604.1:c.*2984C=	ENSP00000514472.1:n.*2984C=
ENST00000699605.1:c.2734C=	ENSP00000514473.1:p.His912=
ENST00000687278.1:c.751C=	ENSP00000509593.1:p.His251=
ENST00000003084.11:c.3160C= MANE Select	ENSP00000003084.6:p.His1054=
ENST00000647720.1:c.810C=
ENST00000648260.1:c.1942C=	ENSP00000497957.1:p.His648=
ENST00000649406.1:c.2977C=	ENSP00000497965.1:p.His993=
ENST00000649781.1:c.2977C=	ENSP00000497203.1:p.His993=
ENST00000003084.10:c.3160C=	ENSP00000003084.6:p.His1054=
ENST00000426809.5:c.3070C=	ENSP00000389119.1:p.His1024=
NM_000492.3:c.3160C= , LRG_663t1:c.3160C=	NP_000483.3:p.His1054=
XM_011515751.1:c.3250C=	XP_011514053.1:p.His1084=
XM_011515752.1:c.3250C=	XP_011514054.1:p.His1084=
XM_011515753.1:c.2917C=	XP_011514055.1:p.His973=
XM_011515754.1:c.2917C=	XP_011514056.1:p.His973=
NM_000492.4:c.3160C= MANE Select	NP_000483.3:p.His1054=