Canonical Allele Identifier: CA1737386673

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611588T= , CM000669.2:g.117611588T=	GRCh38
NC_000007.13:g.117251642T= , CM000669.1:g.117251642T=	GRCh37
NC_000007.12:g.117038878T=	NCBI36
NG_016465.4:g.150805T= , LRG_663:g.150805T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3147T=	ENSP00000497673.2:p.Ser1049=
ENST00000647978.2:c.*2861T=	ENSP00000497658.1:n.*2861T=
ENST00000649781.2:c.2964T=	ENSP00000497203.1:p.Ser988=
ENST00000685018.2:c.3147T=	ENSP00000510194.2:p.Ser1049=
ENST00000687278.2:c.3147T=	ENSP00000509593.2:p.Ser1049=
ENST00000699585.1:c.3147T=	ENSP00000514456.1:p.Ser1049=
ENST00000699598.1:c.3147T=	ENSP00000514467.1:p.Ser1049=
ENST00000699599.1:c.3147T=	ENSP00000514468.1:p.Ser1049=
ENST00000699600.1:c.3147T=	ENSP00000514469.1:p.Ser1049=
ENST00000699601.1:c.*1447T=	ENSP00000514470.1:n.*1447T=
ENST00000699602.1:c.3147T=	ENSP00000514471.1:p.Ser1049=
ENST00000699604.1:c.*2971T=	ENSP00000514472.1:n.*2971T=
ENST00000699605.1:c.2721T=	ENSP00000514473.1:p.Ser907=
ENST00000687278.1:c.738T=	ENSP00000509593.1:p.Ser246=
ENST00000003084.11:c.3147T= MANE Select	ENSP00000003084.6:p.Ser1049=
ENST00000647720.1:c.797T=
ENST00000648260.1:c.1929T=	ENSP00000497957.1:p.Ser643=
ENST00000649406.1:c.2964T=	ENSP00000497965.1:p.Ser988=
ENST00000649781.1:c.2964T=	ENSP00000497203.1:p.Ser988=
ENST00000003084.10:c.3147T=	ENSP00000003084.6:p.Ser1049=
ENST00000426809.5:c.3057T=	ENSP00000389119.1:p.Ser1019=
NM_000492.3:c.3147T= , LRG_663t1:c.3147T=	NP_000483.3:p.Ser1049=
XM_011515751.1:c.3237T=	XP_011514053.1:p.Ser1079=
XM_011515752.1:c.3237T=	XP_011514054.1:p.Ser1079=
XM_011515753.1:c.2904T=	XP_011514055.1:p.Ser968=
XM_011515754.1:c.2904T=	XP_011514056.1:p.Ser968=
NM_000492.4:c.3147T= MANE Select	NP_000483.3:p.Ser1049=