Canonical Allele Identifier: CA1737422976
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117665540A= , CM000669.2:g.117665540A= GRCh38
NC_000007.13:g.117305594A= , CM000669.1:g.117305594A= GRCh37
NC_000007.12:g.117092830A= NCBI36
NG_016465.4:g.204757A= , LRG_663:g.204757A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.*427A= ENSP00000497673.2:n.*427A=
ENST00000647978.2:c.*3932A= ENSP00000497658.1:n.*3932A=
ENST00000649781.2:c.4035A= ENSP00000497203.1:p.Ala1345=
ENST00000685018.2:c.*431A= ENSP00000510194.2:n.*431A=
ENST00000687278.2:c.*871A= ENSP00000509593.2:n.*871A=
ENST00000699585.1:c.*427A= ENSP00000514456.1:n.*427A=
ENST00000699598.1:c.4218A= ENSP00000514467.1:p.Ala1406=
ENST00000699599.1:c.*431A= ENSP00000514468.1:n.*431A=
ENST00000699600.1:c.*879A= ENSP00000514469.1:n.*879A=
ENST00000699601.1:c.*2593A= ENSP00000514470.1:n.*2593A=
ENST00000699602.1:c.4212A= ENSP00000514471.1:p.Ala1404=
ENST00000699604.1:c.*4042A= ENSP00000514472.1:n.*4042A=
ENST00000699605.1:c.3792A= ENSP00000514473.1:p.Ala1264=
ENST00000699606.1:n.2386A=
ENST00000685018.1:c.1082A= ENSP00000510194.1:n.1082A=
ENST00000687278.1:c.2005A= ENSP00000509593.1:n.2005A=
ENST00000689011.1:c.800A=
ENST00000003084.11:c.4218A= MANE Select ENSP00000003084.6:p.Ala1406=
ENST00000647720.1:c.1668A=
ENST00000649781.1:c.4035A= ENSP00000497203.1:p.Ala1345=
ENST00000003084.10:c.4218A= ENSP00000003084.6:p.Ala1406=
ENST00000426809.5:c.4128A= ENSP00000389119.1:p.Ala1376=
ENST00000600166.1:c.344A=
NM_000492.3:c.4218A= , LRG_663t1:c.4218A= NP_000483.3:p.Ala1406=
XM_011515751.1:c.4308A= XP_011514053.1:p.Ala1436=
XM_011515752.1:c.4308A= XP_011514054.1:p.Ala1436=
XM_011515753.1:c.3975A= XP_011514055.1:p.Ala1325=
XM_011515754.1:c.3975A= XP_011514056.1:p.Ala1325=
NM_000492.4:c.4218A= MANE Select NP_000483.3:p.Ala1406=