Canonical Allele Identifier: CA1737390038
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117587744C= , CM000669.2:g.117587744C= GRCh38
NC_000007.13:g.117227798C= , CM000669.1:g.117227798C= GRCh37
NC_000007.12:g.117015034C= NCBI36
NG_016465.4:g.126961C= , LRG_663:g.126961C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.1590C= ENSP00000497673.2:p.Ile530=
ENST00000647978.2:c.*1304C= ENSP00000497658.1:n.*1304C=
ENST00000649781.2:c.1407C= ENSP00000497203.1:p.Ile469=
ENST00000685018.2:c.1590C= ENSP00000510194.2:p.Ile530=
ENST00000687278.2:c.1590C= ENSP00000509593.2:p.Ile530=
ENST00000699585.1:c.1590C= ENSP00000514456.1:p.Ile530=
ENST00000699598.1:c.1590C= ENSP00000514467.1:p.Ile530=
ENST00000699599.1:c.1590C= ENSP00000514468.1:p.Ile530=
ENST00000699600.1:c.1590C= ENSP00000514469.1:p.Ile530=
ENST00000699601.1:c.1590C= ENSP00000514470.1:p.Ile530=
ENST00000699602.1:c.1590C= ENSP00000514471.1:p.Ile530=
ENST00000699604.1:c.*1414C= ENSP00000514472.1:n.*1414C=
ENST00000699605.1:c.1164C= ENSP00000514473.1:p.Ile388=
ENST00000003084.11:c.1590C= MANE Select ENSP00000003084.6:p.Ile530=
ENST00000647978.1:c.*1304C= ENSP00000497658.1:n.*1304C=
ENST00000648260.1:c.1402-15082C= ENSP00000497957.1:n.1402-15082C=
ENST00000649406.1:c.1407C= ENSP00000497965.1:p.Ile469=
ENST00000649781.1:c.1407C= ENSP00000497203.1:p.Ile469=
ENST00000003084.10:c.1590C= ENSP00000003084.6:p.Ile530=
ENST00000426809.5:c.1500C= ENSP00000389119.1:p.Ile500=
ENST00000472848.1:n.143C=
NM_000492.3:c.1590C= , LRG_663t1:c.1590C= NP_000483.3:p.Ile530=
XM_011515751.1:c.1680C= XP_011514053.1:p.Ile560=
XM_011515752.1:c.1680C= XP_011514054.1:p.Ile560=
XM_011515753.1:c.1347C= XP_011514055.1:p.Ile449=
XM_011515754.1:c.1347C= XP_011514056.1:p.Ile449=
NM_000492.4:c.1590C= MANE Select NP_000483.3:p.Ile530=