Canonical Allele Identifier: CA457229472

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117250689A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117610635A>G , CM000669.2:g.117610635A>G	GRCh38
NC_000007.13:g.117250689A>G , CM000669.1:g.117250689A>G	GRCh37
NC_000007.12:g.117037925A>G	NCBI36
NG_016465.4:g.149852A>G , LRG_663:g.149852A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3105A>G	ENSP00000497673.2:p.Gln1035=
ENST00000647978.2:c.*2819A>G	ENSP00000497658.1:n.*2819A>G
ENST00000649781.2:c.2922A>G	ENSP00000497203.1:p.Gln974=
ENST00000685018.2:c.3105A>G	ENSP00000510194.2:p.Gln1035=
ENST00000687278.2:c.3105A>G	ENSP00000509593.2:p.Gln1035=
ENST00000699585.1:c.3105A>G	ENSP00000514456.1:p.Gln1035=
ENST00000699598.1:c.3105A>G	ENSP00000514467.1:p.Gln1035=
ENST00000699599.1:c.3105A>G	ENSP00000514468.1:p.Gln1035=
ENST00000699600.1:c.3105A>G	ENSP00000514469.1:p.Gln1035=
ENST00000699601.1:c.*1405A>G	ENSP00000514470.1:n.*1405A>G
ENST00000699602.1:c.3105A>G	ENSP00000514471.1:p.Gln1035=
ENST00000699604.1:c.*2929A>G	ENSP00000514472.1:n.*2929A>G
ENST00000699605.1:c.2679A>G	ENSP00000514473.1:p.Gln893=
ENST00000687278.1:c.696A>G	ENSP00000509593.1:p.Gln232=
ENST00000003084.11:c.3105A>G MANE Select	ENSP00000003084.6:p.Gln1035=
ENST00000647720.1:c.755A>G
ENST00000648260.1:c.1887A>G	ENSP00000497957.1:p.Gln629=
ENST00000649406.1:c.2922A>G	ENSP00000497965.1:p.Gln974=
ENST00000649781.1:c.2922A>G	ENSP00000497203.1:p.Gln974=
ENST00000003084.10:c.3105A>G	ENSP00000003084.6:p.Gln1035=
ENST00000426809.5:c.3015A>G	ENSP00000389119.1:p.Gln1005=
NM_000492.3:c.3105A>G , LRG_663t1:c.3105A>G	NP_000483.3:p.Gln1035=
XM_011515751.1:c.3195A>G	XP_011514053.1:p.Gln1065=
XM_011515752.1:c.3195A>G	XP_011514054.1:p.Gln1065=
XM_011515753.1:c.2862A>G	XP_011514055.1:p.Gln954=
XM_011515754.1:c.2862A>G	XP_011514056.1:p.Gln954=
NM_000492.4:c.3105A>G MANE Select	NP_000483.3:p.Gln1035=