Canonical Allele Identifier: CA1737392366

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117590393_117590399delinsCCTTTTG , CM000669.2:g.117590393_117590399delinsCCTTTTG	GRCh38
NC_000007.13:g.117230447_117230453delinsCCTTTTG , CM000669.1:g.117230447_117230453delinsCCTTTTG	GRCh37
NC_000007.12:g.117017683_117017689delinsCCTTTTG	NCBI36
NG_016465.4:g.129610_129616delinsCCTTTTG , LRG_663:g.129610_129616delinsCCTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.1720_1726delinsCCTTTTG	ENSP00000497673.2:p.Pro574=
ENST00000647978.2:c.*1434_*1440delinsCCTTTTG	ENSP00000497658.1:n.*1434_*1440delinsCCTTTTG
ENST00000649781.2:c.1537_1543delinsCCTTTTG	ENSP00000497203.1:p.Pro513=
ENST00000685018.2:c.1720_1726delinsCCTTTTG	ENSP00000510194.2:p.Pro574=
ENST00000687278.2:c.1720_1726delinsCCTTTTG	ENSP00000509593.2:p.Pro574=
ENST00000699585.1:c.1720_1726delinsCCTTTTG	ENSP00000514456.1:p.Pro574=
ENST00000699598.1:c.1720_1726delinsCCTTTTG	ENSP00000514467.1:p.Pro574=
ENST00000699599.1:c.1720_1726delinsCCTTTTG	ENSP00000514468.1:p.Pro574=
ENST00000699600.1:c.1720_1726delinsCCTTTTG	ENSP00000514469.1:p.Pro574=
ENST00000699601.1:c.*20_*26delinsCCTTTTG	ENSP00000514470.1:n.*20_*26delinsCCTTTTG
ENST00000699602.1:c.1720_1726delinsCCTTTTG	ENSP00000514471.1:p.Pro574=
ENST00000699604.1:c.*1544_*1550delinsCCTTTTG	ENSP00000514472.1:n.*1544_*1550delinsCCTTTTG
ENST00000699605.1:c.1294_1300delinsCCTTTTG	ENSP00000514473.1:p.Pro432=
ENST00000003084.11:c.1720_1726delinsCCTTTTG MANE Select	ENSP00000003084.6:p.Pro574=
ENST00000647978.1:c.*1434_*1440delinsCCTTTTG	ENSP00000497658.1:n.*1434_*1440delinsCCTTTTG
ENST00000648260.1:c.1402-12433_1402-12427delinsCCTTTTG	ENSP00000497957.1:n.1402-12433_1402-12427delinsCCTTTTG
ENST00000649406.1:c.1537_1543delinsCCTTTTG	ENSP00000497965.1:p.Pro513=
ENST00000649781.1:c.1537_1543delinsCCTTTTG	ENSP00000497203.1:p.Pro513=
ENST00000003084.10:c.1720_1726delinsCCTTTTG	ENSP00000003084.6:p.Pro574=
ENST00000426809.5:c.1630_1636delinsCCTTTTG	ENSP00000389119.1:p.Pro544=
NM_000492.3:c.1720_1726delinsCCTTTTG , LRG_663t1:c.1720_1726delinsCCTTTTG	NP_000483.3:p.Pro574=
XM_011515751.1:c.1810_1816delinsCCTTTTG	XP_011514053.1:p.Pro604=
XM_011515752.1:c.1810_1816delinsCCTTTTG	XP_011514054.1:p.Pro604=
XM_011515753.1:c.1477_1483delinsCCTTTTG	XP_011514055.1:p.Pro493=
XM_011515754.1:c.1477_1483delinsCCTTTTG	XP_011514056.1:p.Pro493=
NM_000492.4:c.1720_1726delinsCCTTTTG MANE Select	NP_000483.3:p.Pro574=