Canonical Allele Identifier: CA1737410845

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117652675C= , CM000669.2:g.117652675C=	GRCh38
NC_000007.13:g.117292729C= , CM000669.1:g.117292729C=	GRCh37
NC_000007.12:g.117079965C=	NCBI36
NG_016465.4:g.191892C= , LRG_663:g.191892C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.*83-167C=	ENSP00000497673.2:n.*83-167C=
ENST00000647978.2:c.*3588-167C=	ENSP00000497658.1:n.*3588-167C=
ENST00000649781.2:c.3691-167C=	ENSP00000497203.1:n.3691-167C=
ENST00000685018.2:c.*87-167C=	ENSP00000510194.2:n.*87-167C=
ENST00000687278.2:c.*527-167C=	ENSP00000509593.2:n.*527-167C=
ENST00000699585.1:c.*83-167C=	ENSP00000514456.1:n.*83-167C=
ENST00000699598.1:c.3874-167C=	ENSP00000514467.1:n.3874-167C=
ENST00000699599.1:c.*87-167C=	ENSP00000514468.1:n.*87-167C=
ENST00000699600.1:c.*535-167C=	ENSP00000514469.1:n.*535-167C=
ENST00000699601.1:c.*2249-167C=	ENSP00000514470.1:n.*2249-167C=
ENST00000699602.1:c.3868-167C=	ENSP00000514471.1:n.3868-167C=
ENST00000699604.1:c.*3698-167C=	ENSP00000514472.1:n.*3698-167C=
ENST00000699605.1:c.3448-167C=	ENSP00000514473.1:n.3448-167C=
ENST00000699606.1:n.1875C=
ENST00000685018.1:c.738-167C=	ENSP00000510194.1:n.738-167C=
ENST00000687278.1:c.1661-167C=	ENSP00000509593.1:n.1661-167C=
ENST00000689011.1:c.456-167C=
ENST00000003084.11:c.3874-167C= MANE Select	ENSP00000003084.6:n.3874-167C=
ENST00000647720.1:c.1324-167C=
ENST00000649781.1:c.3691-167C=	ENSP00000497203.1:n.3691-167C=
ENST00000003084.10:c.3874-167C=	ENSP00000003084.6:n.3874-167C=
ENST00000426809.5:c.3784-167C=	ENSP00000389119.1:n.3784-167C=
NM_000492.3:c.3874-167C= , LRG_663t1:c.3874-167C=	NP_000483.3:n.3874-167C=
XM_011515751.1:c.3964-167C=	XP_011514053.1:n.3964-167C=
XM_011515752.1:c.3964-167C=	XP_011514054.1:n.3964-167C=
XM_011515753.1:c.3631-167C=	XP_011514055.1:n.3631-167C=
XM_011515754.1:c.3631-167C=	XP_011514056.1:n.3631-167C=
NM_000492.4:c.3874-167C= MANE Select	NP_000483.3:n.3874-167C=