Canonical Allele Identifier: CA1737407406
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117666961C= , CM000669.2:g.117666961C= GRCh38
NC_000007.13:g.117307015C= , CM000669.1:g.117307015C= GRCh37
NC_000007.12:g.117094251C= NCBI36
NG_016465.4:g.206178C= , LRG_663:g.206178C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.*505C= ENSP00000497673.2:n.*505C=
ENST00000647978.2:c.*4010C= ENSP00000497658.1:n.*4010C=
ENST00000649781.2:c.4113C= ENSP00000497203.1:p.Asn1371=
ENST00000685018.2:c.*509C= ENSP00000510194.2:n.*509C=
ENST00000687278.2:c.*896-641C= ENSP00000509593.2:n.*896-641C=
ENST00000699585.1:c.*765C= ENSP00000514456.1:n.*765C=
ENST00000699598.1:c.*2C= ENSP00000514467.1:n.*2C=
ENST00000699599.1:c.*509C= ENSP00000514468.1:n.*509C=
ENST00000699600.1:c.*904-641C= ENSP00000514469.1:n.*904-641C=
ENST00000699601.1:c.*2671C= ENSP00000514470.1:n.*2671C=
ENST00000699602.1:c.4290C= ENSP00000514471.1:p.Asn1430=
ENST00000699604.1:c.*4120C= ENSP00000514472.1:n.*4120C=
ENST00000699605.1:c.3870C= ENSP00000514473.1:p.Asn1290=
ENST00000699606.1:n.3807C=
ENST00000685018.1:c.1160C= ENSP00000510194.1:n.1160C=
ENST00000687278.1:c.2030-641C= ENSP00000509593.1:n.2030-641C=
ENST00000689011.1:c.1138C=
ENST00000003084.11:c.4296C= MANE Select ENSP00000003084.6:p.Asn1432=
ENST00000647720.1:c.1746C=
ENST00000649781.1:c.4113C= ENSP00000497203.1:p.Asn1371=
ENST00000003084.10:c.4296C= ENSP00000003084.6:p.Asn1432=
ENST00000426809.5:c.4206C= ENSP00000389119.1:p.Asn1402=
ENST00000600166.1:c.368+1397C=
NM_000492.3:c.4296C= , LRG_663t1:c.4296C= NP_000483.3:p.Asn1432=
XM_011515751.1:c.4386C= XP_011514053.1:p.Asn1462=
XM_011515753.1:c.4053C= XP_011514055.1:p.Asn1351=
XM_011515754.1:c.4053C= XP_011514056.1:p.Asn1351=
NM_000492.4:c.4296C= MANE Select NP_000483.3:p.Asn1432=