Canonical Allele Identifier: CA1737404740
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117642463C= , CM000669.2:g.117642463C= GRCh38
NC_000007.13:g.117282517C= , CM000669.1:g.117282517C= GRCh37
NC_000007.12:g.117069753C= NCBI36
NG_016465.4:g.181680C= , LRG_663:g.181680C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.3543C= ENSP00000497673.2:p.Ile1181=
ENST00000647978.2:c.*3457C= ENSP00000497658.1:n.*3457C=
ENST00000649781.2:c.3560C= ENSP00000497203.1:p.Ser1187=
ENST00000685018.2:c.3743C= ENSP00000510194.2:p.Ser1248=
ENST00000687278.2:c.*396C= ENSP00000509593.2:n.*396C=
ENST00000699585.1:c.3543C= ENSP00000514456.1:p.Ile1181=
ENST00000699598.1:c.3743C= ENSP00000514467.1:p.Ser1248=
ENST00000699599.1:c.3743C= ENSP00000514468.1:p.Ser1248=
ENST00000699600.1:c.*404C= ENSP00000514469.1:n.*404C=
ENST00000699601.1:c.*2118C= ENSP00000514470.1:n.*2118C=
ENST00000699602.1:c.3737C= ENSP00000514471.1:p.Ser1246=
ENST00000699604.1:c.*3567C= ENSP00000514472.1:n.*3567C=
ENST00000699605.1:c.3317C= ENSP00000514473.1:p.Ser1106=
ENST00000685018.1:c.491C= ENSP00000510194.1:p.Ser164=
ENST00000687278.1:c.1530C= ENSP00000509593.1:n.1530C=
ENST00000689011.1:c.325C=
ENST00000003084.11:c.3743C= MANE Select ENSP00000003084.6:p.Ser1248=
ENST00000647720.1:c.1193C=
ENST00000649781.1:c.3560C= ENSP00000497203.1:p.Ser1187=
ENST00000003084.10:c.3743C= ENSP00000003084.6:p.Ser1248=
ENST00000426809.5:c.3653C= ENSP00000389119.1:p.Ser1218=
NM_000492.3:c.3743C= , LRG_663t1:c.3743C= NP_000483.3:p.Ser1248=
XM_011515751.1:c.3833C= XP_011514053.1:p.Ser1278=
XM_011515752.1:c.3833C= XP_011514054.1:p.Ser1278=
XM_011515753.1:c.3500C= XP_011514055.1:p.Ser1167=
XM_011515754.1:c.3500C= XP_011514056.1:p.Ser1167=
NM_000492.4:c.3743C= MANE Select NP_000483.3:p.Ser1248=