Canonical Allele Identifier: CA368993307

Gene: CFTR

Linked Data

• COSMIC: COSM5406301
• MyVariant Identifiers: chr7:g.117254678G>A (hg19) ; chr7:g.117614624G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117614624G>A , CM000669.2:g.117614624G>A	GRCh38
NC_000007.13:g.117254678G>A , CM000669.1:g.117254678G>A	GRCh37
NC_000007.12:g.117041914G>A	NCBI36
NG_016465.4:g.153841G>A , LRG_663:g.153841G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3379G>A	ENSP00000497673.2:p.Gly1127Arg
ENST00000647978.2:c.*3093G>A	ENSP00000497658.1:n.*3093G>A
ENST00000649781.2:c.3196G>A	ENSP00000497203.1:p.Gly1066Arg
ENST00000685018.2:c.3379G>A	ENSP00000510194.2:p.Gly1127Arg
ENST00000687278.2:c.3379G>A	ENSP00000509593.2:p.Gly1127Arg
ENST00000699585.1:c.3379G>A	ENSP00000514456.1:p.Gly1127Arg
ENST00000699598.1:c.3379G>A	ENSP00000514467.1:p.Gly1127Arg
ENST00000699599.1:c.3379G>A	ENSP00000514468.1:p.Gly1127Arg
ENST00000699600.1:c.3379G>A	ENSP00000514469.1:p.Gly1127Arg
ENST00000699601.1:c.*1754G>A	ENSP00000514470.1:n.*1754G>A
ENST00000699602.1:c.3373G>A	ENSP00000514471.1:p.Gly1125Arg
ENST00000699604.1:c.*3203G>A	ENSP00000514472.1:n.*3203G>A
ENST00000699605.1:c.2953G>A	ENSP00000514473.1:p.Gly985Arg
ENST00000685018.1:c.127G>A	ENSP00000510194.1:p.Gly43Arg
ENST00000687278.1:c.970G>A	ENSP00000509593.1:p.Gly324Arg
ENST00000003084.11:c.3379G>A MANE Select	ENSP00000003084.6:p.Gly1127Arg
ENST00000647720.1:c.1029G>A
ENST00000648260.1:c.2161G>A	ENSP00000497957.1:p.Gly721Arg
ENST00000649406.1:c.3196G>A	ENSP00000497965.1:p.Gly1066Arg
ENST00000649781.1:c.3196G>A	ENSP00000497203.1:p.Gly1066Arg
ENST00000003084.10:c.3379G>A	ENSP00000003084.6:p.Gly1127Arg
ENST00000426809.5:c.3289G>A	ENSP00000389119.1:p.Gly1097Arg
ENST00000468795.1:c.204G>A
NM_000492.3:c.3379G>A , LRG_663t1:c.3379G>A	NP_000483.3:p.Gly1127Arg
XM_011515751.1:c.3469G>A	XP_011514053.1:p.Gly1157Arg
XM_011515752.1:c.3469G>A	XP_011514054.1:p.Gly1157Arg
XM_011515753.1:c.3136G>A	XP_011514055.1:p.Gly1046Arg
XM_011515754.1:c.3136G>A	XP_011514056.1:p.Gly1046Arg
NM_000492.4:c.3379G>A MANE Select	NP_000483.3:p.Gly1127Arg