Canonical Allele Identifier: CA368981337
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117592610G>A , CM000669.2:g.117592610G>A GRCh38
NC_000007.13:g.117232664G>A , CM000669.1:g.117232664G>A GRCh37
NC_000007.12:g.117019900G>A NCBI36
NG_016465.4:g.131827G>A , LRG_663:g.131827G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.2443G>A ENSP00000497673.2:p.Glu815Lys
ENST00000647978.2:c.*2157G>A ENSP00000497658.1:n.*2157G>A
ENST00000649781.2:c.2260G>A ENSP00000497203.1:p.Glu754Lys
ENST00000685018.2:c.2443G>A ENSP00000510194.2:p.Glu815Lys
ENST00000687278.2:c.2443G>A ENSP00000509593.2:p.Glu815Lys
ENST00000699585.1:c.2443G>A ENSP00000514456.1:p.Glu815Lys
ENST00000699598.1:c.2443G>A ENSP00000514467.1:p.Glu815Lys
ENST00000699599.1:c.2443G>A ENSP00000514468.1:p.Glu815Lys
ENST00000699600.1:c.2443G>A ENSP00000514469.1:p.Glu815Lys
ENST00000699601.1:c.*743G>A ENSP00000514470.1:n.*743G>A
ENST00000699602.1:c.2443G>A ENSP00000514471.1:p.Glu815Lys
ENST00000699604.1:c.*2267G>A ENSP00000514472.1:n.*2267G>A
ENST00000699605.1:c.2017G>A ENSP00000514473.1:p.Glu673Lys
ENST00000687278.1:c.34G>A ENSP00000509593.1:p.Glu12Lys
ENST00000003084.11:c.2443G>A MANE Select ENSP00000003084.6:p.Glu815Lys
ENST00000647720.1:c.93G>A
ENST00000647978.1:c.*2157G>A ENSP00000497658.1:n.*2157G>A
ENST00000648260.1:c.1402-10216G>A ENSP00000497957.1:n.1402-10216G>A
ENST00000649406.1:c.2260G>A ENSP00000497965.1:p.Glu754Lys
ENST00000649781.1:c.2260G>A ENSP00000497203.1:p.Glu754Lys
ENST00000003084.10:c.2443G>A ENSP00000003084.6:p.Glu815Lys
ENST00000426809.5:c.2353G>A ENSP00000389119.1:p.Glu785Lys
NM_000492.3:c.2443G>A , LRG_663t1:c.2443G>A NP_000483.3:p.Glu815Lys
XM_011515751.1:c.2533G>A XP_011514053.1:p.Glu845Lys
XM_011515752.1:c.2533G>A XP_011514054.1:p.Glu845Lys
XM_011515753.1:c.2200G>A XP_011514055.1:p.Glu734Lys
XM_011515754.1:c.2200G>A XP_011514056.1:p.Glu734Lys
NM_000492.4:c.2443G>A MANE Select NP_000483.3:p.Glu815Lys