Canonical Allele Identifier: CA1737404783
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117642531G= , CM000669.2:g.117642531G= GRCh38
NC_000007.13:g.117282585G= , CM000669.1:g.117282585G= GRCh37
NC_000007.12:g.117069821G= NCBI36
NG_016465.4:g.181748G= , LRG_663:g.181748G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.*20G= ENSP00000497673.2:n.*20G=
ENST00000647978.2:c.*3525G= ENSP00000497658.1:n.*3525G=
ENST00000649781.2:c.3628G= ENSP00000497203.1:p.Gly1210=
ENST00000685018.2:c.3811G= ENSP00000510194.2:p.Gly1271=
ENST00000687278.2:c.*464G= ENSP00000509593.2:n.*464G=
ENST00000699585.1:c.*20G= ENSP00000514456.1:n.*20G=
ENST00000699598.1:c.3811G= ENSP00000514467.1:p.Gly1271=
ENST00000699599.1:c.3811G= ENSP00000514468.1:p.Gly1271=
ENST00000699600.1:c.*472G= ENSP00000514469.1:n.*472G=
ENST00000699601.1:c.*2186G= ENSP00000514470.1:n.*2186G=
ENST00000699602.1:c.3805G= ENSP00000514471.1:p.Gly1269=
ENST00000699604.1:c.*3635G= ENSP00000514472.1:n.*3635G=
ENST00000699605.1:c.3385G= ENSP00000514473.1:p.Gly1129=
ENST00000685018.1:c.559G= ENSP00000510194.1:p.Gly187=
ENST00000687278.1:c.1598G= ENSP00000509593.1:n.1598G=
ENST00000689011.1:c.393G=
ENST00000003084.11:c.3811G= MANE Select ENSP00000003084.6:p.Gly1271=
ENST00000647720.1:c.1261G=
ENST00000649781.1:c.3628G= ENSP00000497203.1:p.Gly1210=
ENST00000003084.10:c.3811G= ENSP00000003084.6:p.Gly1271=
ENST00000426809.5:c.3721G= ENSP00000389119.1:p.Gly1241=
NM_000492.3:c.3811G= , LRG_663t1:c.3811G= NP_000483.3:p.Gly1271=
XM_011515751.1:c.3901G= XP_011514053.1:p.Gly1301=
XM_011515752.1:c.3901G= XP_011514054.1:p.Gly1301=
XM_011515753.1:c.3568G= XP_011514055.1:p.Gly1190=
XM_011515754.1:c.3568G= XP_011514056.1:p.Gly1190=
NM_000492.4:c.3811G= MANE Select NP_000483.3:p.Gly1271=