Canonical Allele Identifier: CA1737404765
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117642498C= , CM000669.2:g.117642498C= GRCh38
NC_000007.13:g.117282552C= , CM000669.1:g.117282552C= GRCh37
NC_000007.12:g.117069788C= NCBI36
NG_016465.4:g.181715C= , LRG_663:g.181715C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.3578C= ENSP00000497673.2:p.Thr1193=
ENST00000647978.2:c.*3492C= ENSP00000497658.1:n.*3492C=
ENST00000649781.2:c.3595C= ENSP00000497203.1:p.Leu1199=
ENST00000685018.2:c.3778C= ENSP00000510194.2:p.Leu1260=
ENST00000687278.2:c.*431C= ENSP00000509593.2:n.*431C=
ENST00000699585.1:c.3578C= ENSP00000514456.1:p.Thr1193=
ENST00000699598.1:c.3778C= ENSP00000514467.1:p.Leu1260=
ENST00000699599.1:c.3778C= ENSP00000514468.1:p.Leu1260=
ENST00000699600.1:c.*439C= ENSP00000514469.1:n.*439C=
ENST00000699601.1:c.*2153C= ENSP00000514470.1:n.*2153C=
ENST00000699602.1:c.3772C= ENSP00000514471.1:p.Leu1258=
ENST00000699604.1:c.*3602C= ENSP00000514472.1:n.*3602C=
ENST00000699605.1:c.3352C= ENSP00000514473.1:p.Leu1118=
ENST00000685018.1:c.526C= ENSP00000510194.1:p.Leu176=
ENST00000687278.1:c.1565C= ENSP00000509593.1:n.1565C=
ENST00000689011.1:c.360C=
ENST00000003084.11:c.3778C= MANE Select ENSP00000003084.6:p.Leu1260=
ENST00000647720.1:c.1228C=
ENST00000649781.1:c.3595C= ENSP00000497203.1:p.Leu1199=
ENST00000003084.10:c.3778C= ENSP00000003084.6:p.Leu1260=
ENST00000426809.5:c.3688C= ENSP00000389119.1:p.Leu1230=
NM_000492.3:c.3778C= , LRG_663t1:c.3778C= NP_000483.3:p.Leu1260=
XM_011515751.1:c.3868C= XP_011514053.1:p.Leu1290=
XM_011515752.1:c.3868C= XP_011514054.1:p.Leu1290=
XM_011515753.1:c.3535C= XP_011514055.1:p.Leu1179=
XM_011515754.1:c.3535C= XP_011514056.1:p.Leu1179=
NM_000492.4:c.3778C= MANE Select NP_000483.3:p.Leu1260=