Canonical Allele Identifier: CA1737394035

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117592027T= , CM000669.2:g.117592027T=	GRCh38
NC_000007.13:g.117232081T= , CM000669.1:g.117232081T=	GRCh37
NC_000007.12:g.117019317T=	NCBI36
NG_016465.4:g.131244T= , LRG_663:g.131244T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.1860T=	ENSP00000497673.2:p.His620=
ENST00000647978.2:c.*1574T=	ENSP00000497658.1:n.*1574T=
ENST00000649781.2:c.1677T=	ENSP00000497203.1:p.His559=
ENST00000685018.2:c.1860T=	ENSP00000510194.2:p.His620=
ENST00000687278.2:c.1860T=	ENSP00000509593.2:p.His620=
ENST00000699585.1:c.1860T=	ENSP00000514456.1:p.His620=
ENST00000699598.1:c.1860T=	ENSP00000514467.1:p.His620=
ENST00000699599.1:c.1860T=	ENSP00000514468.1:p.His620=
ENST00000699600.1:c.1860T=	ENSP00000514469.1:p.His620=
ENST00000699601.1:c.*160T=	ENSP00000514470.1:n.*160T=
ENST00000699602.1:c.1860T=	ENSP00000514471.1:p.His620=
ENST00000699604.1:c.*1684T=	ENSP00000514472.1:n.*1684T=
ENST00000699605.1:c.1434T=	ENSP00000514473.1:p.His478=
ENST00000003084.11:c.1860T= MANE Select	ENSP00000003084.6:p.His620=
ENST00000647978.1:c.*1574T=	ENSP00000497658.1:n.*1574T=
ENST00000648260.1:c.1402-10799T=	ENSP00000497957.1:n.1402-10799T=
ENST00000649406.1:c.1677T=	ENSP00000497965.1:p.His559=
ENST00000649781.1:c.1677T=	ENSP00000497203.1:p.His559=
ENST00000003084.10:c.1860T=	ENSP00000003084.6:p.His620=
ENST00000426809.5:c.1770T=	ENSP00000389119.1:p.His590=
NM_000492.3:c.1860T= , LRG_663t1:c.1860T=	NP_000483.3:p.His620=
XM_011515751.1:c.1950T=	XP_011514053.1:p.His650=
XM_011515752.1:c.1950T=	XP_011514054.1:p.His650=
XM_011515753.1:c.1617T=	XP_011514055.1:p.His539=
XM_011515754.1:c.1617T=	XP_011514056.1:p.His539=
NM_000492.4:c.1860T= MANE Select	NP_000483.3:p.His620=