Canonical Allele Identifier: CA1737411279
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117652913A= , CM000669.2:g.117652913A= GRCh38
NC_000007.13:g.117292967A= , CM000669.1:g.117292967A= GRCh37
NC_000007.12:g.117080203A= NCBI36
NG_016465.4:g.192130A= , LRG_663:g.192130A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.*154A= ENSP00000497673.2:n.*154A=
ENST00000647978.2:c.*3659A= ENSP00000497658.1:n.*3659A=
ENST00000649781.2:c.3762A= ENSP00000497203.1:p.Ile1254=
ENST00000685018.2:c.*158A= ENSP00000510194.2:n.*158A=
ENST00000687278.2:c.*598A= ENSP00000509593.2:n.*598A=
ENST00000699585.1:c.*154A= ENSP00000514456.1:n.*154A=
ENST00000699598.1:c.3945A= ENSP00000514467.1:p.Ile1315=
ENST00000699599.1:c.*158A= ENSP00000514468.1:n.*158A=
ENST00000699600.1:c.*606A= ENSP00000514469.1:n.*606A=
ENST00000699601.1:c.*2320A= ENSP00000514470.1:n.*2320A=
ENST00000699602.1:c.3939A= ENSP00000514471.1:p.Ile1313=
ENST00000699604.1:c.*3769A= ENSP00000514472.1:n.*3769A=
ENST00000699605.1:c.3519A= ENSP00000514473.1:p.Ile1173=
ENST00000699606.1:n.2113A=
ENST00000685018.1:c.809A= ENSP00000510194.1:n.809A=
ENST00000687278.1:c.1732A= ENSP00000509593.1:n.1732A=
ENST00000689011.1:c.527A=
ENST00000003084.11:c.3945A= MANE Select ENSP00000003084.6:p.Ile1315=
ENST00000647720.1:c.1395A=
ENST00000649781.1:c.3762A= ENSP00000497203.1:p.Ile1254=
ENST00000003084.10:c.3945A= ENSP00000003084.6:p.Ile1315=
ENST00000426809.5:c.3855A= ENSP00000389119.1:p.Ile1285=
ENST00000600166.1:c.71A=
NM_000492.3:c.3945A= , LRG_663t1:c.3945A= NP_000483.3:p.Ile1315=
XM_011515751.1:c.4035A= XP_011514053.1:p.Ile1345=
XM_011515752.1:c.4035A= XP_011514054.1:p.Ile1345=
XM_011515753.1:c.3702A= XP_011514055.1:p.Ile1234=
XM_011515754.1:c.3702A= XP_011514056.1:p.Ile1234=
NM_000492.4:c.3945A= MANE Select NP_000483.3:p.Ile1315=