Canonical Allele Identifier: CA368984551

Gene: CFTR CFTR-AS1

Linked Data

• ClinVar Variation Id: 1773566
• ClinVar RCV Id: RCV002397140
• dbSNP Id: rs1466073638
• gnomAD v3: 7-117559551-T-G
• gnomAD v4: 7-117559551-T-G
• MyVariant Identifiers: chr7:g.117199605T>G (hg19) ; chr7:g.117559551T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117559551T>G , CM000669.2:g.117559551T>G	GRCh38
NC_000007.13:g.117199605T>G , CM000669.1:g.117199605T>G	GRCh37
NC_000007.12:g.116986841T>G	NCBI36
NG_016465.4:g.98768T>G , LRG_663:g.98768T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.1480T>G (CFTR)	ENSP00000497673.2:p.Phe494Val
ENST00000647978.2:c.*1194T>G (CFTR)	ENSP00000497658.1:n.*1194T>G
ENST00000649781.2:c.1297T>G (CFTR)	ENSP00000497203.1:p.Phe433Val
ENST00000685018.2:c.1480T>G (CFTR)	ENSP00000510194.2:p.Phe494Val
ENST00000687278.2:c.1480T>G (CFTR)	ENSP00000509593.2:p.Phe494Val
ENST00000699585.1:c.1480T>G (CFTR)	ENSP00000514456.1:p.Phe494Val
ENST00000699596.1:c.1480T>G (CFTR)	ENSP00000514465.1:p.Phe494Val
ENST00000699597.1:c.*38T>G (CFTR)	ENSP00000514466.1:n.*38T>G
ENST00000699598.1:c.1480T>G (CFTR)	ENSP00000514467.1:p.Phe494Val
ENST00000699599.1:c.1480T>G (CFTR)	ENSP00000514468.1:p.Phe494Val
ENST00000699600.1:c.1480T>G (CFTR)	ENSP00000514469.1:p.Phe494Val
ENST00000699601.1:c.1480T>G (CFTR)	ENSP00000514470.1:p.Phe494Val
ENST00000699602.1:c.1480T>G (CFTR)	ENSP00000514471.1:p.Phe494Val
ENST00000699604.1:c.*1304T>G (CFTR)	ENSP00000514472.1:n.*1304T>G
ENST00000699605.1:c.1054T>G (CFTR)	ENSP00000514473.1:p.Phe352Val
ENST00000003084.11:c.1480T>G (CFTR) MANE Select	ENSP00000003084.6:p.Phe494Val
ENST00000647978.1:c.*1194T>G (CFTR)	ENSP00000497658.1:n.*1194T>G
ENST00000648260.1:c.1297T>G (CFTR)	ENSP00000497957.1:p.Phe433Val
ENST00000649406.1:c.1297T>G (CFTR)	ENSP00000497965.1:p.Phe433Val
ENST00000649781.1:c.1297T>G (CFTR)	ENSP00000497203.1:p.Phe433Val
ENST00000003084.10:c.1480T>G (CFTR)	ENSP00000003084.6:p.Phe494Val
ENST00000426809.5:c.1390T>G (CFTR)	ENSP00000389119.1:p.Phe464Val
NM_000492.3:c.1480T>G , LRG_663t1:c.1480T>G (CFTR)	NP_000483.3:p.Phe494Val
XM_011515751.1:c.1570T>G (CFTR)	XP_011514053.1:p.Phe524Val
XM_011515752.1:c.1570T>G (CFTR)	XP_011514054.1:p.Phe524Val
XM_011515753.1:c.1237T>G (CFTR)	XP_011514055.1:p.Phe413Val
XM_011515754.1:c.1237T>G (CFTR)	XP_011514056.1:p.Phe413Val
NR_149084.1:n.221+1182A>C (CFTR-AS1)
NM_000492.4:c.1480T>G (CFTR) MANE Select	NP_000483.3:p.Phe494Val