Canonical Allele Identifier: CA368996028

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117267597T>A (hg19) ; chr7:g.117627543T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117627543T>A , CM000669.2:g.117627543T>A	GRCh38
NC_000007.13:g.117267597T>A , CM000669.1:g.117267597T>A	GRCh37
NC_000007.12:g.117054833T>A	NCBI36
NG_016465.4:g.166760T>A , LRG_663:g.166760T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3490T>A	ENSP00000497673.2:p.Phe1164Ile
ENST00000647978.2:c.*3204T>A	ENSP00000497658.1:n.*3204T>A
ENST00000649781.2:c.3307T>A	ENSP00000497203.1:p.Phe1103Ile
ENST00000685018.2:c.3490T>A	ENSP00000510194.2:p.Phe1164Ile
ENST00000687278.2:c.*143T>A	ENSP00000509593.2:n.*143T>A
ENST00000699585.1:c.3490T>A	ENSP00000514456.1:p.Phe1164Ile
ENST00000699598.1:c.3490T>A	ENSP00000514467.1:p.Phe1164Ile
ENST00000699599.1:c.3490T>A	ENSP00000514468.1:p.Phe1164Ile
ENST00000699600.1:c.*151T>A	ENSP00000514469.1:n.*151T>A
ENST00000699601.1:c.*1865T>A	ENSP00000514470.1:n.*1865T>A
ENST00000699602.1:c.3484T>A	ENSP00000514471.1:p.Phe1162Ile
ENST00000699604.1:c.*3314T>A	ENSP00000514472.1:n.*3314T>A
ENST00000699605.1:c.3064T>A	ENSP00000514473.1:p.Phe1022Ile
ENST00000685018.1:c.238T>A	ENSP00000510194.1:p.Phe80Ile
ENST00000687278.1:c.1277T>A	ENSP00000509593.1:n.1277T>A
ENST00000689011.1:c.72T>A
ENST00000003084.11:c.3490T>A MANE Select	ENSP00000003084.6:p.Phe1164Ile
ENST00000647720.1:c.1140T>A
ENST00000648260.1:c.2272T>A	ENSP00000497957.1:p.Phe758Ile
ENST00000649406.1:c.3307T>A	ENSP00000497965.1:p.Phe1103Ile
ENST00000649781.1:c.3307T>A	ENSP00000497203.1:p.Phe1103Ile
ENST00000003084.10:c.3490T>A	ENSP00000003084.6:p.Phe1164Ile
ENST00000426809.5:c.3400T>A	ENSP00000389119.1:p.Phe1134Ile
ENST00000468795.1:c.315T>A
NM_000492.3:c.3490T>A , LRG_663t1:c.3490T>A	NP_000483.3:p.Phe1164Ile
XM_011515751.1:c.3580T>A	XP_011514053.1:p.Phe1194Ile
XM_011515752.1:c.3580T>A	XP_011514054.1:p.Phe1194Ile
XM_011515753.1:c.3247T>A	XP_011514055.1:p.Phe1083Ile
XM_011515754.1:c.3247T>A	XP_011514056.1:p.Phe1083Ile
NM_000492.4:c.3490T>A MANE Select	NP_000483.3:p.Phe1164Ile