Canonical Allele Identifier: CA457230033

Gene: CFTR

Linked Data

• gnomAD v4: 7-117611675-C-T
• MyVariant Identifiers: chr7:g.117251729C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611675C>T , CM000669.2:g.117611675C>T	GRCh38
NC_000007.13:g.117251729C>T , CM000669.1:g.117251729C>T	GRCh37
NC_000007.12:g.117038965C>T	NCBI36
NG_016465.4:g.150892C>T , LRG_663:g.150892C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3234C>T	ENSP00000497673.2:p.Phe1078=
ENST00000647978.2:c.*2948C>T	ENSP00000497658.1:n.*2948C>T
ENST00000649781.2:c.3051C>T	ENSP00000497203.1:p.Phe1017=
ENST00000685018.2:c.3234C>T	ENSP00000510194.2:p.Phe1078=
ENST00000687278.2:c.3234C>T	ENSP00000509593.2:p.Phe1078=
ENST00000699585.1:c.3234C>T	ENSP00000514456.1:p.Phe1078=
ENST00000699598.1:c.3234C>T	ENSP00000514467.1:p.Phe1078=
ENST00000699599.1:c.3234C>T	ENSP00000514468.1:p.Phe1078=
ENST00000699600.1:c.3234C>T	ENSP00000514469.1:p.Phe1078=
ENST00000699601.1:c.*1534C>T	ENSP00000514470.1:n.*1534C>T
ENST00000699602.1:c.3234C>T	ENSP00000514471.1:p.Phe1078=
ENST00000699604.1:c.*3058C>T	ENSP00000514472.1:n.*3058C>T
ENST00000699605.1:c.2808C>T	ENSP00000514473.1:p.Phe936=
ENST00000687278.1:c.825C>T	ENSP00000509593.1:p.Phe275=
ENST00000003084.11:c.3234C>T MANE Select	ENSP00000003084.6:p.Phe1078=
ENST00000647720.1:c.884C>T
ENST00000648260.1:c.2016C>T	ENSP00000497957.1:p.Phe672=
ENST00000649406.1:c.3051C>T	ENSP00000497965.1:p.Phe1017=
ENST00000649781.1:c.3051C>T	ENSP00000497203.1:p.Phe1017=
ENST00000003084.10:c.3234C>T	ENSP00000003084.6:p.Phe1078=
ENST00000426809.5:c.3144C>T	ENSP00000389119.1:p.Phe1048=
ENST00000468795.1:c.59C>T
NM_000492.3:c.3234C>T , LRG_663t1:c.3234C>T	NP_000483.3:p.Phe1078=
XM_011515751.1:c.3324C>T	XP_011514053.1:p.Phe1108=
XM_011515752.1:c.3324C>T	XP_011514054.1:p.Phe1108=
XM_011515753.1:c.2991C>T	XP_011514055.1:p.Phe997=
XM_011515754.1:c.2991C>T	XP_011514056.1:p.Phe997=
NM_000492.4:c.3234C>T MANE Select	NP_000483.3:p.Phe1078=