Canonical Allele Identifier: CA1737408464

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117668055G= , CM000669.2:g.117668055G=	GRCh38
NC_000007.13:g.117308109G= , CM000669.1:g.117308109G=	GRCh37
NC_000007.12:g.117095345G=	NCBI36
NG_016465.4:g.207272G= , LRG_663:g.207272G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.*1599G=	ENSP00000497673.2:n.*1599G=
ENST00000647978.2:c.*5104G=	ENSP00000497658.1:n.*5104G=
ENST00000649781.2:c.*947G=	ENSP00000497203.1:n.*947G=
ENST00000685018.2:c.*1603G=	ENSP00000510194.2:n.*1603G=
ENST00000687278.2:c.*1051+298G=	ENSP00000509593.2:n.*1051+298G=
ENST00000699585.1:c.*1859G=	ENSP00000514456.1:n.*1859G=
ENST00000699598.1:c.*454+298G=	ENSP00000514467.1:n.*454+298G=
ENST00000699599.1:c.*961+298G=	ENSP00000514468.1:n.*961+298G=
ENST00000699600.1:c.*1059+298G=	ENSP00000514469.1:n.*1059+298G=
ENST00000699601.1:c.*3765G=	ENSP00000514470.1:n.*3765G=
ENST00000699602.1:c.*947G=	ENSP00000514471.1:n.*947G=
ENST00000699604.1:c.*5214G=	ENSP00000514472.1:n.*5214G=
ENST00000699605.1:c.*947G=	ENSP00000514473.1:n.*947G=
ENST00000699606.1:n.4901G=
ENST00000685018.1:c.2254G=	ENSP00000510194.1:n.2254G=
ENST00000687278.1:c.2185+298G=	ENSP00000509593.1:n.2185+298G=
ENST00000689011.1:c.2232G=
ENST00000003084.11:c.*947G= MANE Select	ENSP00000003084.6:n.*947G=
ENST00000647720.1:c.2840G=
ENST00000003084.10:c.*947G=	ENSP00000003084.6:n.*947G=
ENST00000600166.1:c.368+2491G=
NM_000492.3:c.*947G= , LRG_663t1:c.*947G=	NP_000483.3:n.*947G=
XM_011515751.1:c.*947G=	XP_011514053.1:n.*947G=
XM_011515753.1:c.*947G=	XP_011514055.1:n.*947G=
XM_011515754.1:c.*947G=	XP_011514056.1:n.*947G=
NM_000492.4:c.*947G= MANE Select	NP_000483.3:n.*947G=