Canonical Allele Identifier: CA254108
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 38733
dbSNP Id: rs121908757

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117587799A>C , CM000669.2:g.117587799A>C GRCh38
NC_000007.13:g.117227853A>C , CM000669.1:g.117227853A>C GRCh37
NC_000007.12:g.117015089A>C NCBI36
NG_016465.4:g.127016A>C , LRG_663:g.127016A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.1645A>C ENSP00000497673.2:p.Ser549Arg
ENST00000647978.2:c.*1359A>C ENSP00000497658.1:n.*1359A>C
ENST00000649781.2:c.1462A>C ENSP00000497203.1:p.Ser488Arg
ENST00000685018.2:c.1645A>C ENSP00000510194.2:p.Ser549Arg
ENST00000687278.2:c.1645A>C ENSP00000509593.2:p.Ser549Arg
ENST00000699585.1:c.1645A>C ENSP00000514456.1:p.Ser549Arg
ENST00000699598.1:c.1645A>C ENSP00000514467.1:p.Ser549Arg
ENST00000699599.1:c.1645A>C ENSP00000514468.1:p.Ser549Arg
ENST00000699600.1:c.1645A>C ENSP00000514469.1:p.Ser549Arg
ENST00000699601.1:c.1645A>C ENSP00000514470.1:p.Ser549Arg
ENST00000699602.1:c.1645A>C ENSP00000514471.1:p.Ser549Arg
ENST00000699604.1:c.*1469A>C ENSP00000514472.1:n.*1469A>C
ENST00000699605.1:c.1219A>C ENSP00000514473.1:p.Ser407Arg
ENST00000003084.11:c.1645A>C MANE Select ENSP00000003084.6:p.Ser549Arg
ENST00000647978.1:c.*1359A>C ENSP00000497658.1:n.*1359A>C
ENST00000648260.1:c.1402-15027A>C ENSP00000497957.1:n.1402-15027A>C
ENST00000649406.1:c.1462A>C ENSP00000497965.1:p.Ser488Arg
ENST00000649781.1:c.1462A>C ENSP00000497203.1:p.Ser488Arg
ENST00000003084.10:c.1645A>C ENSP00000003084.6:p.Ser549Arg
ENST00000426809.5:c.1555A>C ENSP00000389119.1:p.Ser519Arg
NM_000492.3:c.1645A>C , LRG_663t1:c.1645A>C NP_000483.3:p.Ser549Arg
XM_011515751.1:c.1735A>C XP_011514053.1:p.Ser579Arg
XM_011515752.1:c.1735A>C XP_011514054.1:p.Ser579Arg
XM_011515753.1:c.1402A>C XP_011514055.1:p.Ser468Arg
XM_011515754.1:c.1402A>C XP_011514056.1:p.Ser468Arg
NM_000492.4:c.1645A>C MANE Select NP_000483.3:p.Ser549Arg