Canonical Allele Identifier: CA1737423010
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117665553C= , CM000669.2:g.117665553C= GRCh38
NC_000007.13:g.117305607C= , CM000669.1:g.117305607C= GRCh37
NC_000007.12:g.117092843C= NCBI36
NG_016465.4:g.204770C= , LRG_663:g.204770C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.*440C= ENSP00000497673.2:n.*440C=
ENST00000647978.2:c.*3945C= ENSP00000497658.1:n.*3945C=
ENST00000649781.2:c.4048C= ENSP00000497203.1:p.Gln1350=
ENST00000685018.2:c.*444C= ENSP00000510194.2:n.*444C=
ENST00000687278.2:c.*884C= ENSP00000509593.2:n.*884C=
ENST00000699585.1:c.*440C= ENSP00000514456.1:n.*440C=
ENST00000699598.1:c.4231C= ENSP00000514467.1:p.Gln1411=
ENST00000699599.1:c.*444C= ENSP00000514468.1:n.*444C=
ENST00000699600.1:c.*892C= ENSP00000514469.1:n.*892C=
ENST00000699601.1:c.*2606C= ENSP00000514470.1:n.*2606C=
ENST00000699602.1:c.4225C= ENSP00000514471.1:p.Gln1409=
ENST00000699604.1:c.*4055C= ENSP00000514472.1:n.*4055C=
ENST00000699605.1:c.3805C= ENSP00000514473.1:p.Gln1269=
ENST00000699606.1:n.2399C=
ENST00000685018.1:c.1095C= ENSP00000510194.1:n.1095C=
ENST00000687278.1:c.2018C= ENSP00000509593.1:n.2018C=
ENST00000689011.1:c.813C=
ENST00000003084.11:c.4231C= MANE Select ENSP00000003084.6:p.Gln1411=
ENST00000647720.1:c.1681C=
ENST00000649781.1:c.4048C= ENSP00000497203.1:p.Gln1350=
ENST00000003084.10:c.4231C= ENSP00000003084.6:p.Gln1411=
ENST00000426809.5:c.4141C= ENSP00000389119.1:p.Gln1381=
ENST00000600166.1:c.357C=
NM_000492.3:c.4231C= , LRG_663t1:c.4231C= NP_000483.3:p.Gln1411=
XM_011515751.1:c.4321C= XP_011514053.1:p.Gln1441=
XM_011515752.1:c.4321C= XP_011514054.1:p.Gln1441=
XM_011515753.1:c.3988C= XP_011514055.1:p.Gln1330=
XM_011515754.1:c.3988C= XP_011514056.1:p.Gln1330=
NM_000492.4:c.4231C= MANE Select NP_000483.3:p.Gln1411=