Canonical Allele Identifier: CA1737374525

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603566A= , CM000669.2:g.117603566A=	GRCh38
NC_000007.13:g.117243620A= , CM000669.1:g.117243620A=	GRCh37
NC_000007.12:g.117030856A=	NCBI36
NG_016465.4:g.142783A= , LRG_663:g.142783A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2692A=	ENSP00000497673.2:p.Ser898=
ENST00000647978.2:c.*2406A=	ENSP00000497658.1:n.*2406A=
ENST00000649781.2:c.2509A=	ENSP00000497203.1:p.Ser837=
ENST00000685018.2:c.2692A=	ENSP00000510194.2:p.Ser898=
ENST00000687278.2:c.2692A=	ENSP00000509593.2:p.Ser898=
ENST00000699585.1:c.2692A=	ENSP00000514456.1:p.Ser898=
ENST00000699598.1:c.2692A=	ENSP00000514467.1:p.Ser898=
ENST00000699599.1:c.2692A=	ENSP00000514468.1:p.Ser898=
ENST00000699600.1:c.2692A=	ENSP00000514469.1:p.Ser898=
ENST00000699601.1:c.*992A=	ENSP00000514470.1:n.*992A=
ENST00000699602.1:c.2692A=	ENSP00000514471.1:p.Ser898=
ENST00000699604.1:c.*2516A=	ENSP00000514472.1:n.*2516A=
ENST00000699605.1:c.2266A=	ENSP00000514473.1:p.Ser756=
ENST00000687278.1:c.283A=	ENSP00000509593.1:p.Ser95=
ENST00000003084.11:c.2692A= MANE Select	ENSP00000003084.6:p.Ser898=
ENST00000647720.1:c.342A=
ENST00000648260.1:c.1474A=	ENSP00000497957.1:p.Ser492=
ENST00000649406.1:c.2509A=	ENSP00000497965.1:p.Ser837=
ENST00000649781.1:c.2509A=	ENSP00000497203.1:p.Ser837=
ENST00000003084.10:c.2692A=	ENSP00000003084.6:p.Ser898=
ENST00000426809.5:c.2602A=	ENSP00000389119.1:p.Ser868=
NM_000492.3:c.2692A= , LRG_663t1:c.2692A=	NP_000483.3:p.Ser898=
XM_011515751.1:c.2782A=	XP_011514053.1:p.Ser928=
XM_011515752.1:c.2782A=	XP_011514054.1:p.Ser928=
XM_011515753.1:c.2449A=	XP_011514055.1:p.Ser817=
XM_011515754.1:c.2449A=	XP_011514056.1:p.Ser817=
NM_000492.4:c.2692A= MANE Select	NP_000483.3:p.Ser898=