Canonical Allele Identifier: CA1737395780
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117592650A= , CM000669.2:g.117592650A= GRCh38
NC_000007.13:g.117232704A= , CM000669.1:g.117232704A= GRCh37
NC_000007.12:g.117019940A= NCBI36
NG_016465.4:g.131867A= , LRG_663:g.131867A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.2483A= ENSP00000497673.2:p.Asp828=
ENST00000647978.2:c.*2197A= ENSP00000497658.1:n.*2197A=
ENST00000649781.2:c.2300A= ENSP00000497203.1:p.Asp767=
ENST00000685018.2:c.2483A= ENSP00000510194.2:p.Asp828=
ENST00000687278.2:c.2483A= ENSP00000509593.2:p.Asp828=
ENST00000699585.1:c.2483A= ENSP00000514456.1:p.Asp828=
ENST00000699598.1:c.2483A= ENSP00000514467.1:p.Asp828=
ENST00000699599.1:c.2483A= ENSP00000514468.1:p.Asp828=
ENST00000699600.1:c.2483A= ENSP00000514469.1:p.Asp828=
ENST00000699601.1:c.*783A= ENSP00000514470.1:n.*783A=
ENST00000699602.1:c.2483A= ENSP00000514471.1:p.Asp828=
ENST00000699604.1:c.*2307A= ENSP00000514472.1:n.*2307A=
ENST00000699605.1:c.2057A= ENSP00000514473.1:p.Asp686=
ENST00000687278.1:c.74A= ENSP00000509593.1:p.Asp25=
ENST00000003084.11:c.2483A= MANE Select ENSP00000003084.6:p.Asp828=
ENST00000647720.1:c.133A=
ENST00000647978.1:c.*2197A= ENSP00000497658.1:n.*2197A=
ENST00000648260.1:c.1402-10176A= ENSP00000497957.1:n.1402-10176A=
ENST00000649406.1:c.2300A= ENSP00000497965.1:p.Asp767=
ENST00000649781.1:c.2300A= ENSP00000497203.1:p.Asp767=
ENST00000003084.10:c.2483A= ENSP00000003084.6:p.Asp828=
ENST00000426809.5:c.2393A= ENSP00000389119.1:p.Asp798=
NM_000492.3:c.2483A= , LRG_663t1:c.2483A= NP_000483.3:p.Asp828=
XM_011515751.1:c.2573A= XP_011514053.1:p.Asp858=
XM_011515752.1:c.2573A= XP_011514054.1:p.Asp858=
XM_011515753.1:c.2240A= XP_011514055.1:p.Asp747=
XM_011515754.1:c.2240A= XP_011514056.1:p.Asp747=
NM_000492.4:c.2483A= MANE Select NP_000483.3:p.Asp828=