Canonical Allele Identifier: CA1737394424
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117592164T= , CM000669.2:g.117592164T= GRCh38
NC_000007.13:g.117232218T= , CM000669.1:g.117232218T= GRCh37
NC_000007.12:g.117019454T= NCBI36
NG_016465.4:g.131381T= , LRG_663:g.131381T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.1997T= ENSP00000497673.2:p.Leu666=
ENST00000647978.2:c.*1711T= ENSP00000497658.1:n.*1711T=
ENST00000649781.2:c.1814T= ENSP00000497203.1:p.Leu605=
ENST00000685018.2:c.1997T= ENSP00000510194.2:p.Leu666=
ENST00000687278.2:c.1997T= ENSP00000509593.2:p.Leu666=
ENST00000699585.1:c.1997T= ENSP00000514456.1:p.Leu666=
ENST00000699598.1:c.1997T= ENSP00000514467.1:p.Leu666=
ENST00000699599.1:c.1997T= ENSP00000514468.1:p.Leu666=
ENST00000699600.1:c.1997T= ENSP00000514469.1:p.Leu666=
ENST00000699601.1:c.*297T= ENSP00000514470.1:n.*297T=
ENST00000699602.1:c.1997T= ENSP00000514471.1:p.Leu666=
ENST00000699604.1:c.*1821T= ENSP00000514472.1:n.*1821T=
ENST00000699605.1:c.1571T= ENSP00000514473.1:p.Leu524=
ENST00000003084.11:c.1997T= MANE Select ENSP00000003084.6:p.Leu666=
ENST00000647978.1:c.*1711T= ENSP00000497658.1:n.*1711T=
ENST00000648260.1:c.1402-10662T= ENSP00000497957.1:n.1402-10662T=
ENST00000649406.1:c.1814T= ENSP00000497965.1:p.Leu605=
ENST00000649781.1:c.1814T= ENSP00000497203.1:p.Leu605=
ENST00000003084.10:c.1997T= ENSP00000003084.6:p.Leu666=
ENST00000426809.5:c.1907T= ENSP00000389119.1:p.Leu636=
NM_000492.3:c.1997T= , LRG_663t1:c.1997T= NP_000483.3:p.Leu666=
XM_011515751.1:c.2087T= XP_011514053.1:p.Leu696=
XM_011515752.1:c.2087T= XP_011514054.1:p.Leu696=
XM_011515753.1:c.1754T= XP_011514055.1:p.Leu585=
XM_011515754.1:c.1754T= XP_011514056.1:p.Leu585=
NM_000492.4:c.1997T= MANE Select NP_000483.3:p.Leu666=