Canonical Allele Identifier: CA368987258
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs1397259779

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117603723A>G , CM000669.2:g.117603723A>G GRCh38
NC_000007.13:g.117243777A>G , CM000669.1:g.117243777A>G GRCh37
NC_000007.12:g.117031013A>G NCBI36
NG_016465.4:g.142940A>G , LRG_663:g.142940A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.2849A>G ENSP00000497673.2:p.His950Arg
ENST00000647978.2:c.*2563A>G ENSP00000497658.1:n.*2563A>G
ENST00000649781.2:c.2666A>G ENSP00000497203.1:p.His889Arg
ENST00000685018.2:c.2849A>G ENSP00000510194.2:p.His950Arg
ENST00000687278.2:c.2849A>G ENSP00000509593.2:p.His950Arg
ENST00000699585.1:c.2849A>G ENSP00000514456.1:p.His950Arg
ENST00000699598.1:c.2849A>G ENSP00000514467.1:p.His950Arg
ENST00000699599.1:c.2849A>G ENSP00000514468.1:p.His950Arg
ENST00000699600.1:c.2849A>G ENSP00000514469.1:p.His950Arg
ENST00000699601.1:c.*1149A>G ENSP00000514470.1:n.*1149A>G
ENST00000699602.1:c.2849A>G ENSP00000514471.1:p.His950Arg
ENST00000699604.1:c.*2673A>G ENSP00000514472.1:n.*2673A>G
ENST00000699605.1:c.2423A>G ENSP00000514473.1:p.His808Arg
ENST00000687278.1:c.440A>G ENSP00000509593.1:p.His147Arg
ENST00000003084.11:c.2849A>G MANE Select ENSP00000003084.6:p.His950Arg
ENST00000647720.1:c.499A>G
ENST00000648260.1:c.1631A>G ENSP00000497957.1:p.His544Arg
ENST00000649406.1:c.2666A>G ENSP00000497965.1:p.His889Arg
ENST00000649781.1:c.2666A>G ENSP00000497203.1:p.His889Arg
ENST00000003084.10:c.2849A>G ENSP00000003084.6:p.His950Arg
ENST00000426809.5:c.2759A>G ENSP00000389119.1:p.His920Arg
NM_000492.3:c.2849A>G , LRG_663t1:c.2849A>G NP_000483.3:p.His950Arg
XM_011515751.1:c.2939A>G XP_011514053.1:p.His980Arg
XM_011515752.1:c.2939A>G XP_011514054.1:p.His980Arg
XM_011515753.1:c.2606A>G XP_011514055.1:p.His869Arg
XM_011515754.1:c.2606A>G XP_011514056.1:p.His869Arg
NM_000492.4:c.2849A>G MANE Select NP_000483.3:p.His950Arg