Canonical Allele Identifier: CA2684619420
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117592733A>G , CM000669.2:g.117592733A>G GRCh38
NC_000007.13:g.117232787A>G , CM000669.1:g.117232787A>G GRCh37
NC_000007.12:g.117020023A>G NCBI36
NG_016465.4:g.131950A>G , LRG_663:g.131950A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.2490+76A>G ENSP00000497673.2:n.2490+76A>G
ENST00000647978.2:c.*2204+76A>G ENSP00000497658.1:n.*2204+76A>G
ENST00000649781.2:c.2307+76A>G ENSP00000497203.1:n.2307+76A>G
ENST00000685018.2:c.2490+76A>G ENSP00000510194.2:n.2490+76A>G
ENST00000687278.2:c.2490+76A>G ENSP00000509593.2:n.2490+76A>G
ENST00000699585.1:c.2490+76A>G ENSP00000514456.1:n.2490+76A>G
ENST00000699598.1:c.2490+76A>G ENSP00000514467.1:n.2490+76A>G
ENST00000699599.1:c.2490+76A>G ENSP00000514468.1:n.2490+76A>G
ENST00000699600.1:c.2490+76A>G ENSP00000514469.1:n.2490+76A>G
ENST00000699601.1:c.*790+76A>G ENSP00000514470.1:n.*790+76A>G
ENST00000699602.1:c.2490+76A>G ENSP00000514471.1:n.2490+76A>G
ENST00000699604.1:c.*2314+76A>G ENSP00000514472.1:n.*2314+76A>G
ENST00000699605.1:c.2064+76A>G ENSP00000514473.1:n.2064+76A>G
ENST00000687278.1:c.81+76A>G ENSP00000509593.1:n.81+76A>G
ENST00000003084.11:c.2490+76A>G MANE Select ENSP00000003084.6:n.2490+76A>G
ENST00000647720.1:c.140+76A>G
ENST00000647978.1:c.*2204+76A>G ENSP00000497658.1:n.*2204+76A>G
ENST00000648260.1:c.1402-10093A>G ENSP00000497957.1:n.1402-10093A>G
ENST00000649406.1:c.2307+76A>G ENSP00000497965.1:n.2307+76A>G
ENST00000649781.1:c.2307+76A>G ENSP00000497203.1:n.2307+76A>G
ENST00000003084.10:c.2490+76A>G ENSP00000003084.6:n.2490+76A>G
ENST00000426809.5:c.2400+76A>G ENSP00000389119.1:n.2400+76A>G
NM_000492.3:c.2490+76A>G , LRG_663t1:c.2490+76A>G NP_000483.3:n.2490+76A>G
XM_011515751.1:c.2580+76A>G XP_011514053.1:n.2580+76A>G
XM_011515752.1:c.2580+76A>G XP_011514054.1:n.2580+76A>G
XM_011515753.1:c.2247+76A>G XP_011514055.1:n.2247+76A>G
XM_011515754.1:c.2247+76A>G XP_011514056.1:n.2247+76A>G
NM_000492.4:c.2490+76A>G MANE Select NP_000483.3:n.2490+76A>G