Canonical Allele Identifier: CA2586963938

Gene: CFTR

Linked Data

• ClinVar Variation Id: 2627775
• ClinVar RCV Id: RCV003389119

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117504355_117504362dup , CM000669.2:g.117504355_117504362dup	GRCh38
NC_000007.13:g.117144409_117144416dup , CM000669.1:g.117144409_117144416dup	GRCh37
NC_000007.12:g.116931645_116931652dup	NCBI36
NG_016465.4:g.43572_43579dup , LRG_663:g.43572_43579dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.156_163dup	ENSP00000497673.2:p.Arg55AsnfsTer?
ENST00000647978.2:c.156_163dup	ENSP00000497658.1:p.Arg55AsnfsTer32
ENST00000649781.2:c.156_163dup	ENSP00000497203.1:p.Arg55AsnfsTer?
ENST00000649850.2:c.156_163dup	ENSP00000514457.1:p.Arg55AsnfsTer32
ENST00000685018.2:c.156_163dup	ENSP00000510194.2:p.Arg55AsnfsTer?
ENST00000687278.2:c.156_163dup	ENSP00000509593.2:p.Arg55AsnfsTer?
ENST00000693465.2:n.241_248dup
ENST00000699585.1:c.156_163dup	ENSP00000514456.1:p.Arg55AsnfsTer?
ENST00000699596.1:c.156_163dup	ENSP00000514465.1:p.Arg55AsnfsTer?
ENST00000699597.1:c.156_163dup	ENSP00000514466.1:p.Arg55AsnfsTer?
ENST00000699598.1:c.156_163dup	ENSP00000514467.1:p.Arg55AsnfsTer?
ENST00000699599.1:c.156_163dup	ENSP00000514468.1:p.Arg55AsnfsTer?
ENST00000699600.1:c.156_163dup	ENSP00000514469.1:p.Arg55AsnfsTer?
ENST00000699601.1:c.156_163dup	ENSP00000514470.1:p.Arg55AsnfsTer?
ENST00000699602.1:c.156_163dup	ENSP00000514471.1:p.Arg55AsnfsTer?
ENST00000699604.1:c.156_163dup	ENSP00000514472.1:p.Arg55AsnfsTer?
ENST00000699605.1:c.-88_-81dup	ENSP00000514473.1:n.-88_-81dup
ENST00000446805.2:c.-88_-81dup	ENSP00000417012.1:n.-88_-81dup
ENST00000693465.1:n.226_233dup
ENST00000003084.11:c.156_163dup MANE Select	ENSP00000003084.6:p.Arg55AsnfsTer?
ENST00000647639.1:n.240_247dup
ENST00000647978.1:c.156_163dup	ENSP00000497658.1:p.Arg55AsnfsTer32
ENST00000648260.1:c.156_163dup	ENSP00000497957.1:p.Arg55AsnfsTer?
ENST00000649406.1:c.156_163dup	ENSP00000497965.1:p.Arg55AsnfsTer?
ENST00000649781.1:c.156_163dup	ENSP00000497203.1:p.Arg55AsnfsTer?
ENST00000649850.1:n.239_246dup
ENST00000673785.1:c.-88_-81dup	ENSP00000501235.1:n.-88_-81dup
ENST00000003084.10:c.156_163dup	ENSP00000003084.6:p.Arg55AsnfsTer?
ENST00000426809.5:c.156_163dup	ENSP00000389119.1:p.Arg55AsnfsTer?
ENST00000446805.1:c.-88_-81dup	ENSP00000417012.1:n.-88_-81dup
NM_000492.3:c.156_163dup , LRG_663t1:c.156_163dup	NP_000483.3:p.Arg55AsnfsTer?
XM_011515751.1:c.246_253dup	XP_011514053.1:p.Arg85AsnfsTer?
XM_011515752.1:c.246_253dup	XP_011514054.1:p.Arg85AsnfsTer?
XM_011515753.1:c.-88_-81dup	XP_011514055.1:n.-88_-81dup
XM_011515754.1:c.-162_-155dup	XP_011514056.1:n.-162_-155dup
NM_000492.4:c.156_163dup MANE Select	NP_000483.3:p.Arg55AsnfsTer?