Canonical Allele Identifier: CA368986111

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117242914G>T (hg19) ; chr7:g.117602860G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117602860G>T , CM000669.2:g.117602860G>T	GRCh38
NC_000007.13:g.117242914G>T , CM000669.1:g.117242914G>T	GRCh37
NC_000007.12:g.117030150G>T	NCBI36
NG_016465.4:g.142077G>T , LRG_663:g.142077G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.2654G>T	ENSP00000497673.2:p.Gly885Val
ENST00000647978.2:c.*2368G>T	ENSP00000497658.1:n.*2368G>T
ENST00000649781.2:c.2471G>T	ENSP00000497203.1:p.Gly824Val
ENST00000685018.2:c.2654G>T	ENSP00000510194.2:p.Gly885Val
ENST00000687278.2:c.2654G>T	ENSP00000509593.2:p.Gly885Val
ENST00000699585.1:c.2654G>T	ENSP00000514456.1:p.Gly885Val
ENST00000699598.1:c.2654G>T	ENSP00000514467.1:p.Gly885Val
ENST00000699599.1:c.2654G>T	ENSP00000514468.1:p.Gly885Val
ENST00000699600.1:c.2654G>T	ENSP00000514469.1:p.Gly885Val
ENST00000699601.1:c.*954G>T	ENSP00000514470.1:n.*954G>T
ENST00000699602.1:c.2654G>T	ENSP00000514471.1:p.Gly885Val
ENST00000699604.1:c.*2478G>T	ENSP00000514472.1:n.*2478G>T
ENST00000699605.1:c.2228G>T	ENSP00000514473.1:p.Gly743Val
ENST00000687278.1:c.245G>T	ENSP00000509593.1:p.Gly82Val
ENST00000003084.11:c.2654G>T MANE Select	ENSP00000003084.6:p.Gly885Val
ENST00000647720.1:c.304G>T
ENST00000648260.1:c.1436G>T	ENSP00000497957.1:p.Gly479Val
ENST00000649406.1:c.2471G>T	ENSP00000497965.1:p.Gly824Val
ENST00000649781.1:c.2471G>T	ENSP00000497203.1:p.Gly824Val
ENST00000003084.10:c.2654G>T	ENSP00000003084.6:p.Gly885Val
ENST00000426809.5:c.2564G>T	ENSP00000389119.1:p.Gly855Val
NM_000492.3:c.2654G>T , LRG_663t1:c.2654G>T	NP_000483.3:p.Gly885Val
XM_011515751.1:c.2744G>T	XP_011514053.1:p.Gly915Val
XM_011515752.1:c.2744G>T	XP_011514054.1:p.Gly915Val
XM_011515753.1:c.2411G>T	XP_011514055.1:p.Gly804Val
XM_011515754.1:c.2411G>T	XP_011514056.1:p.Gly804Val
NM_000492.4:c.2654G>T MANE Select	NP_000483.3:p.Gly885Val