Canonical Allele Identifier: CA164962755
Gene: CFTR HGNC NCBI

Linked Data

dbSNP Id: rs945693639

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117668107A>C , CM000669.2:g.117668107A>C GRCh38
NC_000007.13:g.117308161A>C , CM000669.1:g.117308161A>C GRCh37
NC_000007.12:g.117095397A>C NCBI36
NG_016465.4:g.207324A>C , LRG_663:g.207324A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.*1651A>C ENSP00000497673.2:n.*1651A>C
ENST00000647978.2:c.*5156A>C ENSP00000497658.1:n.*5156A>C
ENST00000649781.2:c.*999A>C ENSP00000497203.1:n.*999A>C
ENST00000685018.2:c.*1655A>C ENSP00000510194.2:n.*1655A>C
ENST00000687278.2:c.*1051+350A>C ENSP00000509593.2:n.*1051+350A>C
ENST00000699585.1:c.*1911A>C ENSP00000514456.1:n.*1911A>C
ENST00000699598.1:c.*454+350A>C ENSP00000514467.1:n.*454+350A>C
ENST00000699599.1:c.*961+350A>C ENSP00000514468.1:n.*961+350A>C
ENST00000699600.1:c.*1059+350A>C ENSP00000514469.1:n.*1059+350A>C
ENST00000699601.1:c.*3817A>C ENSP00000514470.1:n.*3817A>C
ENST00000699602.1:c.*999A>C ENSP00000514471.1:n.*999A>C
ENST00000699604.1:c.*5266A>C ENSP00000514472.1:n.*5266A>C
ENST00000699605.1:c.*999A>C ENSP00000514473.1:n.*999A>C
ENST00000699606.1:n.4953A>C
ENST00000685018.1:c.2306A>C ENSP00000510194.1:n.2306A>C
ENST00000687278.1:c.2185+350A>C ENSP00000509593.1:n.2185+350A>C
ENST00000689011.1:c.2284A>C
ENST00000003084.11:c.*999A>C MANE Select ENSP00000003084.6:n.*999A>C
ENST00000647720.1:c.2892A>C
ENST00000003084.10:c.*999A>C ENSP00000003084.6:n.*999A>C
ENST00000600166.1:c.368+2543A>C
NM_000492.3:c.*999A>C , LRG_663t1:c.*999A>C NP_000483.3:n.*999A>C
XM_011515751.1:c.*999A>C XP_011514053.1:n.*999A>C
XM_011515753.1:c.*999A>C XP_011514055.1:n.*999A>C
XM_011515754.1:c.*999A>C XP_011514056.1:n.*999A>C
NM_000492.4:c.*999A>C MANE Select NP_000483.3:n.*999A>C