Canonical Allele Identifier: CA1737362781
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117595035T= , CM000669.2:g.117595035T= GRCh38
NC_000007.13:g.117235089T= , CM000669.1:g.117235089T= GRCh37
NC_000007.12:g.117022325T= NCBI36
NG_016465.4:g.134252T= , LRG_663:g.134252T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.2596T= ENSP00000497673.2:p.Cys866=
ENST00000647978.2:c.*2310T= ENSP00000497658.1:n.*2310T=
ENST00000649781.2:c.2413T= ENSP00000497203.1:p.Cys805=
ENST00000685018.2:c.2596T= ENSP00000510194.2:p.Cys866=
ENST00000687278.2:c.2596T= ENSP00000509593.2:p.Cys866=
ENST00000699585.1:c.2596T= ENSP00000514456.1:p.Cys866=
ENST00000699598.1:c.2596T= ENSP00000514467.1:p.Cys866=
ENST00000699599.1:c.2596T= ENSP00000514468.1:p.Cys866=
ENST00000699600.1:c.2596T= ENSP00000514469.1:p.Cys866=
ENST00000699601.1:c.*896T= ENSP00000514470.1:n.*896T=
ENST00000699602.1:c.2596T= ENSP00000514471.1:p.Cys866=
ENST00000699604.1:c.*2420T= ENSP00000514472.1:n.*2420T=
ENST00000699605.1:c.2170T= ENSP00000514473.1:p.Cys724=
ENST00000687278.1:c.187T= ENSP00000509593.1:p.Cys63=
ENST00000003084.11:c.2596T= MANE Select ENSP00000003084.6:p.Cys866=
ENST00000647720.1:c.246T=
ENST00000648260.1:c.1402-7791T= ENSP00000497957.1:n.1402-7791T=
ENST00000649406.1:c.2413T= ENSP00000497965.1:p.Cys805=
ENST00000649781.1:c.2413T= ENSP00000497203.1:p.Cys805=
ENST00000003084.10:c.2596T= ENSP00000003084.6:p.Cys866=
ENST00000426809.5:c.2506T= ENSP00000389119.1:p.Cys836=
NM_000492.3:c.2596T= , LRG_663t1:c.2596T= NP_000483.3:p.Cys866=
XM_011515751.1:c.2686T= XP_011514053.1:p.Cys896=
XM_011515752.1:c.2686T= XP_011514054.1:p.Cys896=
XM_011515753.1:c.2353T= XP_011514055.1:p.Cys785=
XM_011515754.1:c.2353T= XP_011514056.1:p.Cys785=
NM_000492.4:c.2596T= MANE Select NP_000483.3:p.Cys866=