Canonical Allele Identifier: CA164962463

Gene: CFTR

Linked Data

• ClinVar Variation Id: 639695
• ClinVar RCV Id: RCV000792563 ; RCV002307615 ; RCV001160123
• dbSNP Id: rs748430234
• gnomAD v3: 7-117606711-T-G
• gnomAD v4: 7-117606711-T-G
• MyVariant Identifiers: chr7:g.117246765T>G (hg19) ; chr7:g.117606711T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117606711T>G , CM000669.2:g.117606711T>G	GRCh38
NC_000007.13:g.117246765T>G , CM000669.1:g.117246765T>G	GRCh37
NC_000007.12:g.117034001T>G	NCBI36
NG_016465.4:g.145928T>G , LRG_663:g.145928T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2946T>G	ENSP00000497673.2:p.Ile982Met
ENST00000647978.2:c.*2660T>G	ENSP00000497658.1:n.*2660T>G
ENST00000649781.2:c.2763T>G	ENSP00000497203.1:p.Ile921Met
ENST00000685018.2:c.2946T>G	ENSP00000510194.2:p.Ile982Met
ENST00000687278.2:c.2946T>G	ENSP00000509593.2:p.Ile982Met
ENST00000699585.1:c.2946T>G	ENSP00000514456.1:p.Ile982Met
ENST00000699598.1:c.2946T>G	ENSP00000514467.1:p.Ile982Met
ENST00000699599.1:c.2946T>G	ENSP00000514468.1:p.Ile982Met
ENST00000699600.1:c.2946T>G	ENSP00000514469.1:p.Ile982Met
ENST00000699601.1:c.*1246T>G	ENSP00000514470.1:n.*1246T>G
ENST00000699602.1:c.2946T>G	ENSP00000514471.1:p.Ile982Met
ENST00000699604.1:c.*2770T>G	ENSP00000514472.1:n.*2770T>G
ENST00000699605.1:c.2520T>G	ENSP00000514473.1:p.Ile840Met
ENST00000687278.1:c.537T>G	ENSP00000509593.1:p.Ile179Met
ENST00000003084.11:c.2946T>G MANE Select	ENSP00000003084.6:p.Ile982Met
ENST00000647720.1:c.596T>G
ENST00000648260.1:c.1728T>G	ENSP00000497957.1:p.Ile576Met
ENST00000649406.1:c.2763T>G	ENSP00000497965.1:p.Ile921Met
ENST00000649781.1:c.2763T>G	ENSP00000497203.1:p.Ile921Met
ENST00000003084.10:c.2946T>G	ENSP00000003084.6:p.Ile982Met
ENST00000426809.5:c.2856T>G	ENSP00000389119.1:p.Ile952Met
NM_000492.3:c.2946T>G , LRG_663t1:c.2946T>G	NP_000483.3:p.Ile982Met
XM_011515751.1:c.3036T>G	XP_011514053.1:p.Ile1012Met
XM_011515752.1:c.3036T>G	XP_011514054.1:p.Ile1012Met
XM_011515753.1:c.2703T>G	XP_011514055.1:p.Ile901Met
XM_011515754.1:c.2703T>G	XP_011514056.1:p.Ile901Met
NM_000492.4:c.2946T>G MANE Select	NP_000483.3:p.Ile982Met