Canonical Allele Identifier: CA457449384

Gene: CFTR

Linked Data

• ClinVar Variation Id: 1148421
• ClinVar RCV Id: RCV001488277
• dbSNP Id: rs2116032144
• MyVariant Identifiers: chr7:g.117232372T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117592318T>G , CM000669.2:g.117592318T>G	GRCh38
NC_000007.13:g.117232372T>G , CM000669.1:g.117232372T>G	GRCh37
NC_000007.12:g.117019608T>G	NCBI36
NG_016465.4:g.131535T>G , LRG_663:g.131535T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.2151T>G	ENSP00000497673.2:p.Thr717=
ENST00000647978.2:c.*1865T>G	ENSP00000497658.1:n.*1865T>G
ENST00000649781.2:c.1968T>G	ENSP00000497203.1:p.Thr656=
ENST00000685018.2:c.2151T>G	ENSP00000510194.2:p.Thr717=
ENST00000687278.2:c.2151T>G	ENSP00000509593.2:p.Thr717=
ENST00000699585.1:c.2151T>G	ENSP00000514456.1:p.Thr717=
ENST00000699598.1:c.2151T>G	ENSP00000514467.1:p.Thr717=
ENST00000699599.1:c.2151T>G	ENSP00000514468.1:p.Thr717=
ENST00000699600.1:c.2151T>G	ENSP00000514469.1:p.Thr717=
ENST00000699601.1:c.*451T>G	ENSP00000514470.1:n.*451T>G
ENST00000699602.1:c.2151T>G	ENSP00000514471.1:p.Thr717=
ENST00000699604.1:c.*1975T>G	ENSP00000514472.1:n.*1975T>G
ENST00000699605.1:c.1725T>G	ENSP00000514473.1:p.Thr575=
ENST00000003084.11:c.2151T>G MANE Select	ENSP00000003084.6:p.Thr717=
ENST00000647978.1:c.*1865T>G	ENSP00000497658.1:n.*1865T>G
ENST00000648260.1:c.1402-10508T>G	ENSP00000497957.1:n.1402-10508T>G
ENST00000649406.1:c.1968T>G	ENSP00000497965.1:p.Thr656=
ENST00000649781.1:c.1968T>G	ENSP00000497203.1:p.Thr656=
ENST00000003084.10:c.2151T>G	ENSP00000003084.6:p.Thr717=
ENST00000426809.5:c.2061T>G	ENSP00000389119.1:p.Thr687=
NM_000492.3:c.2151T>G , LRG_663t1:c.2151T>G	NP_000483.3:p.Thr717=
XM_011515751.1:c.2241T>G	XP_011514053.1:p.Thr747=
XM_011515752.1:c.2241T>G	XP_011514054.1:p.Thr747=
XM_011515753.1:c.1908T>G	XP_011514055.1:p.Thr636=
XM_011515754.1:c.1908T>G	XP_011514056.1:p.Thr636=
NM_000492.4:c.2151T>G MANE Select	NP_000483.3:p.Thr717=