Canonical Allele Identifier: CA368975489

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117282623G>T (hg19) ; chr7:g.117642569G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117642569G>T , CM000669.2:g.117642569G>T	GRCh38
NC_000007.13:g.117282623G>T , CM000669.1:g.117282623G>T	GRCh37
NC_000007.12:g.117069859G>T	NCBI36
NG_016465.4:g.181786G>T , LRG_663:g.181786G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.*58G>T	ENSP00000497673.2:n.*58G>T
ENST00000647978.2:c.*3563G>T	ENSP00000497658.1:n.*3563G>T
ENST00000649781.2:c.3666G>T	ENSP00000497203.1:p.Arg1222Ser
ENST00000685018.2:c.3849G>T	ENSP00000510194.2:p.Arg1283Ser
ENST00000687278.2:c.*502G>T	ENSP00000509593.2:n.*502G>T
ENST00000699585.1:c.*58G>T	ENSP00000514456.1:n.*58G>T
ENST00000699598.1:c.3849G>T	ENSP00000514467.1:p.Arg1283Ser
ENST00000699599.1:c.3849G>T	ENSP00000514468.1:p.Arg1283Ser
ENST00000699600.1:c.*510G>T	ENSP00000514469.1:n.*510G>T
ENST00000699601.1:c.*2224G>T	ENSP00000514470.1:n.*2224G>T
ENST00000699602.1:c.3843G>T	ENSP00000514471.1:p.Arg1281Ser
ENST00000699604.1:c.*3673G>T	ENSP00000514472.1:n.*3673G>T
ENST00000699605.1:c.3423G>T	ENSP00000514473.1:p.Arg1141Ser
ENST00000685018.1:c.597G>T	ENSP00000510194.1:p.Arg199Ser
ENST00000687278.1:c.1636G>T	ENSP00000509593.1:n.1636G>T
ENST00000689011.1:c.431G>T
ENST00000003084.11:c.3849G>T MANE Select	ENSP00000003084.6:p.Arg1283Ser
ENST00000647720.1:c.1299G>T
ENST00000649781.1:c.3666G>T	ENSP00000497203.1:p.Arg1222Ser
ENST00000003084.10:c.3849G>T	ENSP00000003084.6:p.Arg1283Ser
ENST00000426809.5:c.3759G>T	ENSP00000389119.1:p.Arg1253Ser
NM_000492.3:c.3849G>T , LRG_663t1:c.3849G>T	NP_000483.3:p.Arg1283Ser
XM_011515751.1:c.3939G>T	XP_011514053.1:p.Arg1313Ser
XM_011515752.1:c.3939G>T	XP_011514054.1:p.Arg1313Ser
XM_011515753.1:c.3606G>T	XP_011514055.1:p.Arg1202Ser
XM_011515754.1:c.3606G>T	XP_011514056.1:p.Arg1202Ser
NM_000492.4:c.3849G>T MANE Select	NP_000483.3:p.Arg1283Ser