Canonical Allele Identifier: CA368992066

Gene: CFTR

Linked Data

• ClinVar Variation Id: 2808233
• ClinVar RCV Id: RCV003618356
• gnomAD v4: 7-117611643-T-G
• MyVariant Identifiers: chr7:g.117251697T>G (hg19) ; chr7:g.117611643T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611643T>G , CM000669.2:g.117611643T>G	GRCh38
NC_000007.13:g.117251697T>G , CM000669.1:g.117251697T>G	GRCh37
NC_000007.12:g.117038933T>G	NCBI36
NG_016465.4:g.150860T>G , LRG_663:g.150860T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3202T>G	ENSP00000497673.2:p.Phe1068Val
ENST00000647978.2:c.*2916T>G	ENSP00000497658.1:n.*2916T>G
ENST00000649781.2:c.3019T>G	ENSP00000497203.1:p.Phe1007Val
ENST00000685018.2:c.3202T>G	ENSP00000510194.2:p.Phe1068Val
ENST00000687278.2:c.3202T>G	ENSP00000509593.2:p.Phe1068Val
ENST00000699585.1:c.3202T>G	ENSP00000514456.1:p.Phe1068Val
ENST00000699598.1:c.3202T>G	ENSP00000514467.1:p.Phe1068Val
ENST00000699599.1:c.3202T>G	ENSP00000514468.1:p.Phe1068Val
ENST00000699600.1:c.3202T>G	ENSP00000514469.1:p.Phe1068Val
ENST00000699601.1:c.*1502T>G	ENSP00000514470.1:n.*1502T>G
ENST00000699602.1:c.3202T>G	ENSP00000514471.1:p.Phe1068Val
ENST00000699604.1:c.*3026T>G	ENSP00000514472.1:n.*3026T>G
ENST00000699605.1:c.2776T>G	ENSP00000514473.1:p.Phe926Val
ENST00000687278.1:c.793T>G	ENSP00000509593.1:p.Phe265Val
ENST00000003084.11:c.3202T>G MANE Select	ENSP00000003084.6:p.Phe1068Val
ENST00000647720.1:c.852T>G
ENST00000648260.1:c.1984T>G	ENSP00000497957.1:p.Phe662Val
ENST00000649406.1:c.3019T>G	ENSP00000497965.1:p.Phe1007Val
ENST00000649781.1:c.3019T>G	ENSP00000497203.1:p.Phe1007Val
ENST00000003084.10:c.3202T>G	ENSP00000003084.6:p.Phe1068Val
ENST00000426809.5:c.3112T>G	ENSP00000389119.1:p.Phe1038Val
ENST00000468795.1:c.27T>G
NM_000492.3:c.3202T>G , LRG_663t1:c.3202T>G	NP_000483.3:p.Phe1068Val
XM_011515751.1:c.3292T>G	XP_011514053.1:p.Phe1098Val
XM_011515752.1:c.3292T>G	XP_011514054.1:p.Phe1098Val
XM_011515753.1:c.2959T>G	XP_011514055.1:p.Phe987Val
XM_011515754.1:c.2959T>G	XP_011514056.1:p.Phe987Val
NM_000492.4:c.3202T>G MANE Select	NP_000483.3:p.Phe1068Val