Canonical Allele Identifier: CA368976048

Gene: CFTR

Linked Data

• ClinVar Variation Id: 1777031
• ClinVar RCV Id: RCV002403544
• gnomAD v4: 7-117587794-C-G
• MyVariant Identifiers: chr7:g.117227848C>G (hg19) ; chr7:g.117587794C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117587794C>G , CM000669.2:g.117587794C>G	GRCh38
NC_000007.13:g.117227848C>G , CM000669.1:g.117227848C>G	GRCh37
NC_000007.12:g.117015084C>G	NCBI36
NG_016465.4:g.127011C>G , LRG_663:g.127011C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.1640C>G	ENSP00000497673.2:p.Thr547Arg
ENST00000647978.2:c.*1354C>G	ENSP00000497658.1:n.*1354C>G
ENST00000649781.2:c.1457C>G	ENSP00000497203.1:p.Thr486Arg
ENST00000685018.2:c.1640C>G	ENSP00000510194.2:p.Thr547Arg
ENST00000687278.2:c.1640C>G	ENSP00000509593.2:p.Thr547Arg
ENST00000699585.1:c.1640C>G	ENSP00000514456.1:p.Thr547Arg
ENST00000699598.1:c.1640C>G	ENSP00000514467.1:p.Thr547Arg
ENST00000699599.1:c.1640C>G	ENSP00000514468.1:p.Thr547Arg
ENST00000699600.1:c.1640C>G	ENSP00000514469.1:p.Thr547Arg
ENST00000699601.1:c.1640C>G	ENSP00000514470.1:p.Thr547Arg
ENST00000699602.1:c.1640C>G	ENSP00000514471.1:p.Thr547Arg
ENST00000699604.1:c.*1464C>G	ENSP00000514472.1:n.*1464C>G
ENST00000699605.1:c.1214C>G	ENSP00000514473.1:p.Thr405Arg
ENST00000003084.11:c.1640C>G MANE Select	ENSP00000003084.6:p.Thr547Arg
ENST00000647978.1:c.*1354C>G	ENSP00000497658.1:n.*1354C>G
ENST00000648260.1:c.1402-15032C>G	ENSP00000497957.1:n.1402-15032C>G
ENST00000649406.1:c.1457C>G	ENSP00000497965.1:p.Thr486Arg
ENST00000649781.1:c.1457C>G	ENSP00000497203.1:p.Thr486Arg
ENST00000003084.10:c.1640C>G	ENSP00000003084.6:p.Thr547Arg
ENST00000426809.5:c.1550C>G	ENSP00000389119.1:p.Thr517Arg
NM_000492.3:c.1640C>G , LRG_663t1:c.1640C>G	NP_000483.3:p.Thr547Arg
XM_011515751.1:c.1730C>G	XP_011514053.1:p.Thr577Arg
XM_011515752.1:c.1730C>G	XP_011514054.1:p.Thr577Arg
XM_011515753.1:c.1397C>G	XP_011514055.1:p.Thr466Arg
XM_011515754.1:c.1397C>G	XP_011514056.1:p.Thr466Arg
NM_000492.4:c.1640C>G MANE Select	NP_000483.3:p.Thr547Arg