Canonical Allele Identifier: CA368975109

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117282584T>G (hg19) ; chr7:g.117642530T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117642530T>G , CM000669.2:g.117642530T>G	GRCh38
NC_000007.13:g.117282584T>G , CM000669.1:g.117282584T>G	GRCh37
NC_000007.12:g.117069820T>G	NCBI36
NG_016465.4:g.181747T>G , LRG_663:g.181747T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.*19T>G	ENSP00000497673.2:n.*19T>G
ENST00000647978.2:c.*3524T>G	ENSP00000497658.1:n.*3524T>G
ENST00000649781.2:c.3627T>G	ENSP00000497203.1:p.Asp1209Glu
ENST00000685018.2:c.3810T>G	ENSP00000510194.2:p.Asp1270Glu
ENST00000687278.2:c.*463T>G	ENSP00000509593.2:n.*463T>G
ENST00000699585.1:c.*19T>G	ENSP00000514456.1:n.*19T>G
ENST00000699598.1:c.3810T>G	ENSP00000514467.1:p.Asp1270Glu
ENST00000699599.1:c.3810T>G	ENSP00000514468.1:p.Asp1270Glu
ENST00000699600.1:c.*471T>G	ENSP00000514469.1:n.*471T>G
ENST00000699601.1:c.*2185T>G	ENSP00000514470.1:n.*2185T>G
ENST00000699602.1:c.3804T>G	ENSP00000514471.1:p.Asp1268Glu
ENST00000699604.1:c.*3634T>G	ENSP00000514472.1:n.*3634T>G
ENST00000699605.1:c.3384T>G	ENSP00000514473.1:p.Asp1128Glu
ENST00000685018.1:c.558T>G	ENSP00000510194.1:p.Asp186Glu
ENST00000687278.1:c.1597T>G	ENSP00000509593.1:n.1597T>G
ENST00000689011.1:c.392T>G
ENST00000003084.11:c.3810T>G MANE Select	ENSP00000003084.6:p.Asp1270Glu
ENST00000647720.1:c.1260T>G
ENST00000649781.1:c.3627T>G	ENSP00000497203.1:p.Asp1209Glu
ENST00000003084.10:c.3810T>G	ENSP00000003084.6:p.Asp1270Glu
ENST00000426809.5:c.3720T>G	ENSP00000389119.1:p.Asp1240Glu
NM_000492.3:c.3810T>G , LRG_663t1:c.3810T>G	NP_000483.3:p.Asp1270Glu
XM_011515751.1:c.3900T>G	XP_011514053.1:p.Asp1300Glu
XM_011515752.1:c.3900T>G	XP_011514054.1:p.Asp1300Glu
XM_011515753.1:c.3567T>G	XP_011514055.1:p.Asp1189Glu
XM_011515754.1:c.3567T>G	XP_011514056.1:p.Asp1189Glu
NM_000492.4:c.3810T>G MANE Select	NP_000483.3:p.Asp1270Glu