Canonical Allele Identifier: CA327085

Gene: CFTR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611637C>A , CM000669.2:g.117611637C>A	GRCh38
NC_000007.13:g.117251691C>A , CM000669.1:g.117251691C>A	GRCh37
NC_000007.12:g.117038927C>A	NCBI36
NG_016465.4:g.150854C>A , LRG_663:g.150854C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3196C>A	ENSP00000497673.2:p.Arg1066Ser
ENST00000647978.2:c.*2910C>A	ENSP00000497658.1:n.*2910C>A
ENST00000649781.2:c.3013C>A	ENSP00000497203.1:p.Arg1005Ser
ENST00000685018.2:c.3196C>A	ENSP00000510194.2:p.Arg1066Ser
ENST00000687278.2:c.3196C>A	ENSP00000509593.2:p.Arg1066Ser
ENST00000699585.1:c.3196C>A	ENSP00000514456.1:p.Arg1066Ser
ENST00000699598.1:c.3196C>A	ENSP00000514467.1:p.Arg1066Ser
ENST00000699599.1:c.3196C>A	ENSP00000514468.1:p.Arg1066Ser
ENST00000699600.1:c.3196C>A	ENSP00000514469.1:p.Arg1066Ser
ENST00000699601.1:c.*1496C>A	ENSP00000514470.1:n.*1496C>A
ENST00000699602.1:c.3196C>A	ENSP00000514471.1:p.Arg1066Ser
ENST00000699604.1:c.*3020C>A	ENSP00000514472.1:n.*3020C>A
ENST00000699605.1:c.2770C>A	ENSP00000514473.1:p.Arg924Ser
ENST00000687278.1:c.787C>A	ENSP00000509593.1:p.Arg263Ser
ENST00000003084.11:c.3196C>A MANE Select	ENSP00000003084.6:p.Arg1066Ser
ENST00000647720.1:c.846C>A
ENST00000648260.1:c.1978C>A	ENSP00000497957.1:p.Arg660Ser
ENST00000649406.1:c.3013C>A	ENSP00000497965.1:p.Arg1005Ser
ENST00000649781.1:c.3013C>A	ENSP00000497203.1:p.Arg1005Ser
ENST00000003084.10:c.3196C>A	ENSP00000003084.6:p.Arg1066Ser
ENST00000426809.5:c.3106C>A	ENSP00000389119.1:p.Arg1036Ser
ENST00000468795.1:c.21C>A
NM_000492.3:c.3196C>A , LRG_663t1:c.3196C>A	NP_000483.3:p.Arg1066Ser
XM_011515751.1:c.3286C>A	XP_011514053.1:p.Arg1096Ser
XM_011515752.1:c.3286C>A	XP_011514054.1:p.Arg1096Ser
XM_011515753.1:c.2953C>A	XP_011514055.1:p.Arg985Ser
XM_011515754.1:c.2953C>A	XP_011514056.1:p.Arg985Ser
NM_000492.4:c.3196C>A MANE Select	NP_000483.3:p.Arg1066Ser