Canonical Allele Identifier: CA368990859

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117250720G>A (hg19) ; chr7:g.117610666G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117610666G>A , CM000669.2:g.117610666G>A	GRCh38
NC_000007.13:g.117250720G>A , CM000669.1:g.117250720G>A	GRCh37
NC_000007.12:g.117037956G>A	NCBI36
NG_016465.4:g.149883G>A , LRG_663:g.149883G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3136G>A	ENSP00000497673.2:p.Glu1046Lys
ENST00000647978.2:c.*2850G>A	ENSP00000497658.1:n.*2850G>A
ENST00000649781.2:c.2953G>A	ENSP00000497203.1:p.Glu985Lys
ENST00000685018.2:c.3136G>A	ENSP00000510194.2:p.Glu1046Lys
ENST00000687278.2:c.3136G>A	ENSP00000509593.2:p.Glu1046Lys
ENST00000699585.1:c.3136G>A	ENSP00000514456.1:p.Glu1046Lys
ENST00000699598.1:c.3136G>A	ENSP00000514467.1:p.Glu1046Lys
ENST00000699599.1:c.3136G>A	ENSP00000514468.1:p.Glu1046Lys
ENST00000699600.1:c.3136G>A	ENSP00000514469.1:p.Glu1046Lys
ENST00000699601.1:c.*1436G>A	ENSP00000514470.1:n.*1436G>A
ENST00000699602.1:c.3136G>A	ENSP00000514471.1:p.Glu1046Lys
ENST00000699604.1:c.*2960G>A	ENSP00000514472.1:n.*2960G>A
ENST00000699605.1:c.2710G>A	ENSP00000514473.1:p.Glu904Lys
ENST00000687278.1:c.727G>A	ENSP00000509593.1:p.Glu243Lys
ENST00000003084.11:c.3136G>A MANE Select	ENSP00000003084.6:p.Glu1046Lys
ENST00000647720.1:c.786G>A
ENST00000648260.1:c.1918G>A	ENSP00000497957.1:p.Glu640Lys
ENST00000649406.1:c.2953G>A	ENSP00000497965.1:p.Glu985Lys
ENST00000649781.1:c.2953G>A	ENSP00000497203.1:p.Glu985Lys
ENST00000003084.10:c.3136G>A	ENSP00000003084.6:p.Glu1046Lys
ENST00000426809.5:c.3046G>A	ENSP00000389119.1:p.Glu1016Lys
NM_000492.3:c.3136G>A , LRG_663t1:c.3136G>A	NP_000483.3:p.Glu1046Lys
XM_011515751.1:c.3226G>A	XP_011514053.1:p.Glu1076Lys
XM_011515752.1:c.3226G>A	XP_011514054.1:p.Glu1076Lys
XM_011515753.1:c.2893G>A	XP_011514055.1:p.Glu965Lys
XM_011515754.1:c.2893G>A	XP_011514056.1:p.Glu965Lys
NM_000492.4:c.3136G>A MANE Select	NP_000483.3:p.Glu1046Lys