Canonical Allele Identifier: CA1737408448

Gene: CFTR

Linked Data

• dbSNP Id: rs1793412071

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117668003G>A , CM000669.2:g.117668003G>A	GRCh38
NC_000007.13:g.117308057G>A , CM000669.1:g.117308057G>A	GRCh37
NC_000007.12:g.117095293G>A	NCBI36
NG_016465.4:g.207220G>A , LRG_663:g.207220G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.*1547G>A	ENSP00000497673.2:n.*1547G>A
ENST00000647978.2:c.*5052G>A	ENSP00000497658.1:n.*5052G>A
ENST00000649781.2:c.*895G>A	ENSP00000497203.1:n.*895G>A
ENST00000685018.2:c.*1551G>A	ENSP00000510194.2:n.*1551G>A
ENST00000687278.2:c.*1051+246G>A	ENSP00000509593.2:n.*1051+246G>A
ENST00000699585.1:c.*1807G>A	ENSP00000514456.1:n.*1807G>A
ENST00000699598.1:c.*454+246G>A	ENSP00000514467.1:n.*454+246G>A
ENST00000699599.1:c.*961+246G>A	ENSP00000514468.1:n.*961+246G>A
ENST00000699600.1:c.*1059+246G>A	ENSP00000514469.1:n.*1059+246G>A
ENST00000699601.1:c.*3713G>A	ENSP00000514470.1:n.*3713G>A
ENST00000699602.1:c.*895G>A	ENSP00000514471.1:n.*895G>A
ENST00000699604.1:c.*5162G>A	ENSP00000514472.1:n.*5162G>A
ENST00000699605.1:c.*895G>A	ENSP00000514473.1:n.*895G>A
ENST00000699606.1:n.4849G>A
ENST00000685018.1:c.2202G>A	ENSP00000510194.1:n.2202G>A
ENST00000687278.1:c.2185+246G>A	ENSP00000509593.1:n.2185+246G>A
ENST00000689011.1:c.2180G>A
ENST00000003084.11:c.*895G>A MANE Select	ENSP00000003084.6:n.*895G>A
ENST00000647720.1:c.2788G>A
ENST00000003084.10:c.*895G>A	ENSP00000003084.6:n.*895G>A
ENST00000600166.1:c.368+2439G>A
NM_000492.3:c.*895G>A , LRG_663t1:c.*895G>A	NP_000483.3:n.*895G>A
XM_011515751.1:c.*895G>A	XP_011514053.1:n.*895G>A
XM_011515753.1:c.*895G>A	XP_011514055.1:n.*895G>A
XM_011515754.1:c.*895G>A	XP_011514056.1:n.*895G>A
NM_000492.4:c.*895G>A MANE Select	NP_000483.3:n.*895G>A