Canonical Allele Identifier: CA457228038

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117243814A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603760A>G , CM000669.2:g.117603760A>G	GRCh38
NC_000007.13:g.117243814A>G , CM000669.1:g.117243814A>G	GRCh37
NC_000007.12:g.117031050A>G	NCBI36
NG_016465.4:g.142977A>G , LRG_663:g.142977A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2886A>G	ENSP00000497673.2:p.Ser962=
ENST00000647978.2:c.*2600A>G	ENSP00000497658.1:n.*2600A>G
ENST00000649781.2:c.2703A>G	ENSP00000497203.1:p.Ser901=
ENST00000685018.2:c.2886A>G	ENSP00000510194.2:p.Ser962=
ENST00000687278.2:c.2886A>G	ENSP00000509593.2:p.Ser962=
ENST00000699585.1:c.2886A>G	ENSP00000514456.1:p.Ser962=
ENST00000699598.1:c.2886A>G	ENSP00000514467.1:p.Ser962=
ENST00000699599.1:c.2886A>G	ENSP00000514468.1:p.Ser962=
ENST00000699600.1:c.2886A>G	ENSP00000514469.1:p.Ser962=
ENST00000699601.1:c.*1186A>G	ENSP00000514470.1:n.*1186A>G
ENST00000699602.1:c.2886A>G	ENSP00000514471.1:p.Ser962=
ENST00000699604.1:c.*2710A>G	ENSP00000514472.1:n.*2710A>G
ENST00000699605.1:c.2460A>G	ENSP00000514473.1:p.Ser820=
ENST00000687278.1:c.477A>G	ENSP00000509593.1:p.Ser159=
ENST00000003084.11:c.2886A>G MANE Select	ENSP00000003084.6:p.Ser962=
ENST00000647720.1:c.536A>G
ENST00000648260.1:c.1668A>G	ENSP00000497957.1:p.Ser556=
ENST00000649406.1:c.2703A>G	ENSP00000497965.1:p.Ser901=
ENST00000649781.1:c.2703A>G	ENSP00000497203.1:p.Ser901=
ENST00000003084.10:c.2886A>G	ENSP00000003084.6:p.Ser962=
ENST00000426809.5:c.2796A>G	ENSP00000389119.1:p.Ser932=
NM_000492.3:c.2886A>G , LRG_663t1:c.2886A>G	NP_000483.3:p.Ser962=
XM_011515751.1:c.2976A>G	XP_011514053.1:p.Ser992=
XM_011515752.1:c.2976A>G	XP_011514054.1:p.Ser992=
XM_011515753.1:c.2643A>G	XP_011514055.1:p.Ser881=
XM_011515754.1:c.2643A>G	XP_011514056.1:p.Ser881=
NM_000492.4:c.2886A>G MANE Select	NP_000483.3:p.Ser962=