Canonical Allele Identifier: CA457449013

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117232255C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117592201C>T , CM000669.2:g.117592201C>T	GRCh38
NC_000007.13:g.117232255C>T , CM000669.1:g.117232255C>T	GRCh37
NC_000007.12:g.117019491C>T	NCBI36
NG_016465.4:g.131418C>T , LRG_663:g.131418C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2034C>T	ENSP00000497673.2:p.Ser678=
ENST00000647978.2:c.*1748C>T	ENSP00000497658.1:n.*1748C>T
ENST00000649781.2:c.1851C>T	ENSP00000497203.1:p.Ser617=
ENST00000685018.2:c.2034C>T	ENSP00000510194.2:p.Ser678=
ENST00000687278.2:c.2034C>T	ENSP00000509593.2:p.Ser678=
ENST00000699585.1:c.2034C>T	ENSP00000514456.1:p.Ser678=
ENST00000699598.1:c.2034C>T	ENSP00000514467.1:p.Ser678=
ENST00000699599.1:c.2034C>T	ENSP00000514468.1:p.Ser678=
ENST00000699600.1:c.2034C>T	ENSP00000514469.1:p.Ser678=
ENST00000699601.1:c.*334C>T	ENSP00000514470.1:n.*334C>T
ENST00000699602.1:c.2034C>T	ENSP00000514471.1:p.Ser678=
ENST00000699604.1:c.*1858C>T	ENSP00000514472.1:n.*1858C>T
ENST00000699605.1:c.1608C>T	ENSP00000514473.1:p.Ser536=
ENST00000003084.11:c.2034C>T MANE Select	ENSP00000003084.6:p.Ser678=
ENST00000647978.1:c.*1748C>T	ENSP00000497658.1:n.*1748C>T
ENST00000648260.1:c.1402-10625C>T	ENSP00000497957.1:n.1402-10625C>T
ENST00000649406.1:c.1851C>T	ENSP00000497965.1:p.Ser617=
ENST00000649781.1:c.1851C>T	ENSP00000497203.1:p.Ser617=
ENST00000003084.10:c.2034C>T	ENSP00000003084.6:p.Ser678=
ENST00000426809.5:c.1944C>T	ENSP00000389119.1:p.Ser648=
NM_000492.3:c.2034C>T , LRG_663t1:c.2034C>T	NP_000483.3:p.Ser678=
XM_011515751.1:c.2124C>T	XP_011514053.1:p.Ser708=
XM_011515752.1:c.2124C>T	XP_011514054.1:p.Ser708=
XM_011515753.1:c.1791C>T	XP_011514055.1:p.Ser597=
XM_011515754.1:c.1791C>T	XP_011514056.1:p.Ser597=
NM_000492.4:c.2034C>T MANE Select	NP_000483.3:p.Ser678=