Canonical Allele Identifier: CA457228073

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117282521G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117642467G>T , CM000669.2:g.117642467G>T	GRCh38
NC_000007.13:g.117282521G>T , CM000669.1:g.117282521G>T	GRCh37
NC_000007.12:g.117069757G>T	NCBI36
NG_016465.4:g.181684G>T , LRG_663:g.181684G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3547G>T	ENSP00000497673.2:p.Glu1183Ter
ENST00000647978.2:c.*3461G>T	ENSP00000497658.1:n.*3461G>T
ENST00000649781.2:c.3564G>T	ENSP00000497203.1:p.Gly1188=
ENST00000685018.2:c.3747G>T	ENSP00000510194.2:p.Gly1249=
ENST00000687278.2:c.*400G>T	ENSP00000509593.2:n.*400G>T
ENST00000699585.1:c.3547G>T	ENSP00000514456.1:p.Glu1183Ter
ENST00000699598.1:c.3747G>T	ENSP00000514467.1:p.Gly1249=
ENST00000699599.1:c.3747G>T	ENSP00000514468.1:p.Gly1249=
ENST00000699600.1:c.*408G>T	ENSP00000514469.1:n.*408G>T
ENST00000699601.1:c.*2122G>T	ENSP00000514470.1:n.*2122G>T
ENST00000699602.1:c.3741G>T	ENSP00000514471.1:p.Gly1247=
ENST00000699604.1:c.*3571G>T	ENSP00000514472.1:n.*3571G>T
ENST00000699605.1:c.3321G>T	ENSP00000514473.1:p.Gly1107=
ENST00000685018.1:c.495G>T	ENSP00000510194.1:p.Gly165=
ENST00000687278.1:c.1534G>T	ENSP00000509593.1:n.1534G>T
ENST00000689011.1:c.329G>T
ENST00000003084.11:c.3747G>T MANE Select	ENSP00000003084.6:p.Gly1249=
ENST00000647720.1:c.1197G>T
ENST00000649781.1:c.3564G>T	ENSP00000497203.1:p.Gly1188=
ENST00000003084.10:c.3747G>T	ENSP00000003084.6:p.Gly1249=
ENST00000426809.5:c.3657G>T	ENSP00000389119.1:p.Gly1219=
NM_000492.3:c.3747G>T , LRG_663t1:c.3747G>T	NP_000483.3:p.Gly1249=
XM_011515751.1:c.3837G>T	XP_011514053.1:p.Gly1279=
XM_011515752.1:c.3837G>T	XP_011514054.1:p.Gly1279=
XM_011515753.1:c.3504G>T	XP_011514055.1:p.Gly1168=
XM_011515754.1:c.3504G>T	XP_011514056.1:p.Gly1168=
NM_000492.4:c.3747G>T MANE Select	NP_000483.3:p.Gly1249=