Canonical Allele Identifier: CA368987472

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117603750del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603750del , CM000669.2:g.117603750del	GRCh38
NC_000007.13:g.117243804del , CM000669.1:g.117243804del	GRCh37
NC_000007.12:g.117031040del	NCBI36
NG_016465.4:g.142967del , LRG_663:g.142967del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.2876del	ENSP00000497673.2:p.Ala959AspfsTer9
ENST00000647978.2:c.*2590del	ENSP00000497658.1:n.*2590del
ENST00000649781.2:c.2693del	ENSP00000497203.1:p.Ala898AspfsTer9
ENST00000685018.2:c.2876del	ENSP00000510194.2:p.Ala959AspfsTer9
ENST00000687278.2:c.2876del	ENSP00000509593.2:p.Ala959AspfsTer9
ENST00000699585.1:c.2876del	ENSP00000514456.1:p.Ala959AspfsTer9
ENST00000699598.1:c.2876del	ENSP00000514467.1:p.Ala959AspfsTer9
ENST00000699599.1:c.2876del	ENSP00000514468.1:p.Ala959AspfsTer9
ENST00000699600.1:c.2876del	ENSP00000514469.1:p.Ala959AspfsTer9
ENST00000699601.1:c.*1176del	ENSP00000514470.1:n.*1176del
ENST00000699602.1:c.2876del	ENSP00000514471.1:p.Ala959AspfsTer9
ENST00000699604.1:c.*2700del	ENSP00000514472.1:n.*2700del
ENST00000699605.1:c.2450del	ENSP00000514473.1:p.Ala817AspfsTer9
ENST00000687278.1:c.467del	ENSP00000509593.1:p.Ala156AspfsTer9
ENST00000003084.11:c.2876del MANE Select	ENSP00000003084.6:p.Ala959AspfsTer9
ENST00000647720.1:c.526del
ENST00000648260.1:c.1658del	ENSP00000497957.1:p.Ala553AspfsTer9
ENST00000649406.1:c.2693del	ENSP00000497965.1:p.Ala898AspfsTer9
ENST00000649781.1:c.2693del	ENSP00000497203.1:p.Ala898AspfsTer9
ENST00000003084.10:c.2876del	ENSP00000003084.6:p.Ala959AspfsTer9
ENST00000426809.5:c.2786del	ENSP00000389119.1:p.Ala929AspfsTer9
NM_000492.3:c.2876del , LRG_663t1:c.2876del	NP_000483.3:p.Ala959AspfsTer9
XM_011515751.1:c.2966del	XP_011514053.1:p.Ala989AspfsTer9
XM_011515752.1:c.2966del	XP_011514054.1:p.Ala989AspfsTer9
XM_011515753.1:c.2633del	XP_011514055.1:p.Ala878AspfsTer9
XM_011515754.1:c.2633del	XP_011514056.1:p.Ala878AspfsTer9
NM_000492.4:c.2876del MANE Select	NP_000483.3:p.Ala959AspfsTer9