Canonical Allele Identifier: CA1737395639
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117592607C= , CM000669.2:g.117592607C= GRCh38
NC_000007.13:g.117232661C= , CM000669.1:g.117232661C= GRCh37
NC_000007.12:g.117019897C= NCBI36
NG_016465.4:g.131824C= , LRG_663:g.131824C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.2440C= ENSP00000497673.2:p.Gln814=
ENST00000647978.2:c.*2154C= ENSP00000497658.1:n.*2154C=
ENST00000649781.2:c.2257C= ENSP00000497203.1:p.Gln753=
ENST00000685018.2:c.2440C= ENSP00000510194.2:p.Gln814=
ENST00000687278.2:c.2440C= ENSP00000509593.2:p.Gln814=
ENST00000699585.1:c.2440C= ENSP00000514456.1:p.Gln814=
ENST00000699598.1:c.2440C= ENSP00000514467.1:p.Gln814=
ENST00000699599.1:c.2440C= ENSP00000514468.1:p.Gln814=
ENST00000699600.1:c.2440C= ENSP00000514469.1:p.Gln814=
ENST00000699601.1:c.*740C= ENSP00000514470.1:n.*740C=
ENST00000699602.1:c.2440C= ENSP00000514471.1:p.Gln814=
ENST00000699604.1:c.*2264C= ENSP00000514472.1:n.*2264C=
ENST00000699605.1:c.2014C= ENSP00000514473.1:p.Gln672=
ENST00000687278.1:c.31C= ENSP00000509593.1:p.Gln11=
ENST00000003084.11:c.2440C= MANE Select ENSP00000003084.6:p.Gln814=
ENST00000647720.1:c.90C=
ENST00000647978.1:c.*2154C= ENSP00000497658.1:n.*2154C=
ENST00000648260.1:c.1402-10219C= ENSP00000497957.1:n.1402-10219C=
ENST00000649406.1:c.2257C= ENSP00000497965.1:p.Gln753=
ENST00000649781.1:c.2257C= ENSP00000497203.1:p.Gln753=
ENST00000003084.10:c.2440C= ENSP00000003084.6:p.Gln814=
ENST00000426809.5:c.2350C= ENSP00000389119.1:p.Gln784=
NM_000492.3:c.2440C= , LRG_663t1:c.2440C= NP_000483.3:p.Gln814=
XM_011515751.1:c.2530C= XP_011514053.1:p.Gln844=
XM_011515752.1:c.2530C= XP_011514054.1:p.Gln844=
XM_011515753.1:c.2197C= XP_011514055.1:p.Gln733=
XM_011515754.1:c.2197C= XP_011514056.1:p.Gln733=
NM_000492.4:c.2440C= MANE Select NP_000483.3:p.Gln814=