Canonical Allele Identifier: CA658683489

Gene: CFTR

Linked Data

• ClinVar Variation Id: 495952
• ClinVar RCV Id: RCV000589412 ; RCV001829626
• dbSNP Id: rs121908771
• MyVariant Identifiers: chr7:g.117174371dup (hg19) ; chr7:g.117534317dup (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117534317dup , CM000669.2:g.117534317dup	GRCh38
NC_000007.13:g.117174371dup , CM000669.1:g.117174371dup	GRCh37
NC_000007.12:g.116961607dup	NCBI36
NG_016465.4:g.73534dup , LRG_663:g.73534dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.531dup	ENSP00000497673.2:p.Gly178TrpfsTer5
ENST00000647978.2:c.*428dup	ENSP00000497658.1:n.*428dup
ENST00000649781.2:c.531dup	ENSP00000497203.1:p.Gly178TrpfsTer5
ENST00000685018.2:c.531dup	ENSP00000510194.2:p.Gly178TrpfsTer5
ENST00000687278.2:c.531dup	ENSP00000509593.2:p.Gly178TrpfsTer5
ENST00000699585.1:c.531dup	ENSP00000514456.1:p.Gly178TrpfsTer5
ENST00000699596.1:c.531dup	ENSP00000514465.1:p.Gly178TrpfsTer5
ENST00000699597.1:c.531dup	ENSP00000514466.1:p.Gly178TrpfsTer5
ENST00000699598.1:c.531dup	ENSP00000514467.1:p.Gly178TrpfsTer5
ENST00000699599.1:c.531dup	ENSP00000514468.1:p.Gly178TrpfsTer5
ENST00000699600.1:c.531dup	ENSP00000514469.1:p.Gly178TrpfsTer5
ENST00000699601.1:c.531dup	ENSP00000514470.1:p.Gly178TrpfsTer5
ENST00000699602.1:c.531dup	ENSP00000514471.1:p.Gly178TrpfsTer5
ENST00000699604.1:c.*355dup	ENSP00000514472.1:n.*355dup
ENST00000699605.1:c.288dup	ENSP00000514473.1:p.Gly97TrpfsTer5
ENST00000003084.11:c.531dup MANE Select	ENSP00000003084.6:p.Gly178TrpfsTer5
ENST00000647978.1:c.*428dup	ENSP00000497658.1:n.*428dup
ENST00000648260.1:c.531dup	ENSP00000497957.1:p.Gly178TrpfsTer5
ENST00000649406.1:c.531dup	ENSP00000497965.1:p.Gly178TrpfsTer5
ENST00000649781.1:c.531dup	ENSP00000497203.1:p.Gly178TrpfsTer5
ENST00000673785.1:c.288dup	ENSP00000501235.1:p.Gly97TrpfsTer5
ENST00000003084.10:c.531dup	ENSP00000003084.6:p.Gly178TrpfsTer5
ENST00000426809.5:c.490-931dup	ENSP00000389119.1:n.490-931dup
NM_000492.3:c.531dup , LRG_663t1:c.531dup	NP_000483.3:p.Gly178TrpfsTer5
XM_011515751.1:c.621dup	XP_011514053.1:p.Gly208TrpfsTer5
XM_011515752.1:c.621dup	XP_011514054.1:p.Gly208TrpfsTer5
XM_011515753.1:c.288dup	XP_011514055.1:p.Gly97TrpfsTer5
XM_011515754.1:c.288dup	XP_011514056.1:p.Gly97TrpfsTer5
NM_000492.4:c.531dup MANE Select	NP_000483.3:p.Gly178TrpfsTer5