Canonical Allele Identifier: CA326727
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs397508329

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117592177dup , CM000669.2:g.117592177dup GRCh38
NC_000007.13:g.117232231dup , CM000669.1:g.117232231dup GRCh37
NC_000007.12:g.117019467dup NCBI36
NG_016465.4:g.131394dup , LRG_663:g.131394dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.2010dup ENSP00000497673.2:p.Leu671IlefsTer18
ENST00000647978.2:c.*1724dup ENSP00000497658.1:n.*1724dup
ENST00000649781.2:c.1827dup ENSP00000497203.1:p.Leu610IlefsTer18
ENST00000685018.2:c.2010dup ENSP00000510194.2:p.Leu671IlefsTer18
ENST00000687278.2:c.2010dup ENSP00000509593.2:p.Leu671IlefsTer18
ENST00000699585.1:c.2010dup ENSP00000514456.1:p.Leu671IlefsTer18
ENST00000699598.1:c.2010dup ENSP00000514467.1:p.Leu671IlefsTer18
ENST00000699599.1:c.2010dup ENSP00000514468.1:p.Leu671IlefsTer18
ENST00000699600.1:c.2010dup ENSP00000514469.1:p.Leu671IlefsTer18
ENST00000699601.1:c.*310dup ENSP00000514470.1:n.*310dup
ENST00000699602.1:c.2010dup ENSP00000514471.1:p.Leu671IlefsTer18
ENST00000699604.1:c.*1834dup ENSP00000514472.1:n.*1834dup
ENST00000699605.1:c.1584dup ENSP00000514473.1:p.Leu529IlefsTer18
ENST00000003084.11:c.2010dup MANE Select ENSP00000003084.6:p.Leu671IlefsTer18
ENST00000647978.1:c.*1724dup ENSP00000497658.1:n.*1724dup
ENST00000648260.1:c.1402-10649dup ENSP00000497957.1:n.1402-10649dup
ENST00000649406.1:c.1827dup ENSP00000497965.1:p.Leu610IlefsTer18
ENST00000649781.1:c.1827dup ENSP00000497203.1:p.Leu610IlefsTer18
ENST00000003084.10:c.2010dup ENSP00000003084.6:p.Leu671IlefsTer18
ENST00000426809.5:c.1920dup ENSP00000389119.1:p.Leu641IlefsTer18
NM_000492.3:c.2010dup , LRG_663t1:c.2010dup NP_000483.3:p.Leu671IlefsTer18
XM_011515751.1:c.2100dup XP_011514053.1:p.Leu701IlefsTer18
XM_011515752.1:c.2100dup XP_011514054.1:p.Leu701IlefsTer18
XM_011515753.1:c.1767dup XP_011514055.1:p.Leu590IlefsTer18
XM_011515754.1:c.1767dup XP_011514056.1:p.Leu590IlefsTer18
NM_000492.4:c.2010dup MANE Select NP_000483.3:p.Leu671IlefsTer18