Canonical Allele Identifier: CA1737408462

Gene: CFTR

Linked Data

• dbSNP Id: rs1793415805
• gnomAD v4: 7-117668041-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117668041G>A , CM000669.2:g.117668041G>A	GRCh38
NC_000007.13:g.117308095G>A , CM000669.1:g.117308095G>A	GRCh37
NC_000007.12:g.117095331G>A	NCBI36
NG_016465.4:g.207258G>A , LRG_663:g.207258G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.*1585G>A	ENSP00000497673.2:n.*1585G>A
ENST00000647978.2:c.*5090G>A	ENSP00000497658.1:n.*5090G>A
ENST00000649781.2:c.*933G>A	ENSP00000497203.1:n.*933G>A
ENST00000685018.2:c.*1589G>A	ENSP00000510194.2:n.*1589G>A
ENST00000687278.2:c.*1051+284G>A	ENSP00000509593.2:n.*1051+284G>A
ENST00000699585.1:c.*1845G>A	ENSP00000514456.1:n.*1845G>A
ENST00000699598.1:c.*454+284G>A	ENSP00000514467.1:n.*454+284G>A
ENST00000699599.1:c.*961+284G>A	ENSP00000514468.1:n.*961+284G>A
ENST00000699600.1:c.*1059+284G>A	ENSP00000514469.1:n.*1059+284G>A
ENST00000699601.1:c.*3751G>A	ENSP00000514470.1:n.*3751G>A
ENST00000699602.1:c.*933G>A	ENSP00000514471.1:n.*933G>A
ENST00000699604.1:c.*5200G>A	ENSP00000514472.1:n.*5200G>A
ENST00000699605.1:c.*933G>A	ENSP00000514473.1:n.*933G>A
ENST00000699606.1:n.4887G>A
ENST00000685018.1:c.2240G>A	ENSP00000510194.1:n.2240G>A
ENST00000687278.1:c.2185+284G>A	ENSP00000509593.1:n.2185+284G>A
ENST00000689011.1:c.2218G>A
ENST00000003084.11:c.*933G>A MANE Select	ENSP00000003084.6:n.*933G>A
ENST00000647720.1:c.2826G>A
ENST00000003084.10:c.*933G>A	ENSP00000003084.6:n.*933G>A
ENST00000600166.1:c.368+2477G>A
NM_000492.3:c.*933G>A , LRG_663t1:c.*933G>A	NP_000483.3:n.*933G>A
XM_011515751.1:c.*933G>A	XP_011514053.1:n.*933G>A
XM_011515753.1:c.*933G>A	XP_011514055.1:n.*933G>A
XM_011515754.1:c.*933G>A	XP_011514056.1:n.*933G>A
NM_000492.4:c.*933G>A MANE Select	NP_000483.3:n.*933G>A