Canonical Allele Identifier: CA325552

Gene: CFTR

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117587833G>A , CM000669.2:g.117587833G>A	GRCh38
NC_000007.13:g.117227887G>A , CM000669.1:g.117227887G>A	GRCh37
NC_000007.12:g.117015123G>A	NCBI36
NG_016465.4:g.127050G>A , LRG_663:g.127050G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.1679G>A	ENSP00000497673.2:p.Arg560Lys
ENST00000647978.2:c.*1393G>A	ENSP00000497658.1:n.*1393G>A
ENST00000649781.2:c.1496G>A	ENSP00000497203.1:p.Arg499Lys
ENST00000685018.2:c.1679G>A	ENSP00000510194.2:p.Arg560Lys
ENST00000687278.2:c.1679G>A	ENSP00000509593.2:p.Arg560Lys
ENST00000699585.1:c.1679G>A	ENSP00000514456.1:p.Arg560Lys
ENST00000699598.1:c.1679G>A	ENSP00000514467.1:p.Arg560Lys
ENST00000699599.1:c.1679G>A	ENSP00000514468.1:p.Arg560Lys
ENST00000699600.1:c.1679G>A	ENSP00000514469.1:p.Arg560Lys
ENST00000699601.1:c.1679G>A	ENSP00000514470.1:p.Ser560Asn
ENST00000699602.1:c.1679G>A	ENSP00000514471.1:p.Arg560Lys
ENST00000699604.1:c.*1503G>A	ENSP00000514472.1:n.*1503G>A
ENST00000699605.1:c.1253G>A	ENSP00000514473.1:p.Arg418Lys
ENST00000003084.11:c.1679G>A MANE Select	ENSP00000003084.6:p.Arg560Lys
ENST00000647978.1:c.*1393G>A	ENSP00000497658.1:n.*1393G>A
ENST00000648260.1:c.1402-14993G>A	ENSP00000497957.1:n.1402-14993G>A
ENST00000649406.1:c.1496G>A	ENSP00000497965.1:p.Arg499Lys
ENST00000649781.1:c.1496G>A	ENSP00000497203.1:p.Arg499Lys
ENST00000003084.10:c.1679G>A	ENSP00000003084.6:p.Arg560Lys
ENST00000426809.5:c.1589G>A	ENSP00000389119.1:p.Arg530Lys
NM_000492.3:c.1679G>A , LRG_663t1:c.1679G>A	NP_000483.3:p.Arg560Lys
XM_011515751.1:c.1769G>A	XP_011514053.1:p.Arg590Lys
XM_011515752.1:c.1769G>A	XP_011514054.1:p.Arg590Lys
XM_011515753.1:c.1436G>A	XP_011514055.1:p.Arg479Lys
XM_011515754.1:c.1436G>A	XP_011514056.1:p.Arg479Lys
NM_000492.4:c.1679G>A MANE Select	NP_000483.3:p.Arg560Lys