Canonical Allele Identifier: CA457231197

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117267635C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117627581C>A , CM000669.2:g.117627581C>A	GRCh38
NC_000007.13:g.117267635C>A , CM000669.1:g.117267635C>A	GRCh37
NC_000007.12:g.117054871C>A	NCBI36
NG_016465.4:g.166798C>A , LRG_663:g.166798C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3517+11C>A	ENSP00000497673.2:n.3517+11C>A
ENST00000647978.2:c.*3242C>A	ENSP00000497658.1:n.*3242C>A
ENST00000649781.2:c.3345C>A	ENSP00000497203.1:p.Thr1115=
ENST00000685018.2:c.3528C>A	ENSP00000510194.2:p.Thr1176=
ENST00000687278.2:c.*181C>A	ENSP00000509593.2:n.*181C>A
ENST00000699585.1:c.3517+11C>A	ENSP00000514456.1:n.3517+11C>A
ENST00000699598.1:c.3528C>A	ENSP00000514467.1:p.Thr1176=
ENST00000699599.1:c.3528C>A	ENSP00000514468.1:p.Thr1176=
ENST00000699600.1:c.*189C>A	ENSP00000514469.1:n.*189C>A
ENST00000699601.1:c.*1903C>A	ENSP00000514470.1:n.*1903C>A
ENST00000699602.1:c.3522C>A	ENSP00000514471.1:p.Thr1174=
ENST00000699604.1:c.*3352C>A	ENSP00000514472.1:n.*3352C>A
ENST00000699605.1:c.3102C>A	ENSP00000514473.1:p.Thr1034=
ENST00000685018.1:c.276C>A	ENSP00000510194.1:p.Thr92=
ENST00000687278.1:c.1315C>A	ENSP00000509593.1:n.1315C>A
ENST00000689011.1:c.110C>A
ENST00000003084.11:c.3528C>A MANE Select	ENSP00000003084.6:p.Thr1176=
ENST00000647720.1:c.1167+11C>A
ENST00000648260.1:c.2310C>A	ENSP00000497957.1:p.Thr770=
ENST00000649406.1:c.3345C>A	ENSP00000497965.1:p.Thr1115=
ENST00000649781.1:c.3345C>A	ENSP00000497203.1:p.Thr1115=
ENST00000003084.10:c.3528C>A	ENSP00000003084.6:p.Thr1176=
ENST00000426809.5:c.3438C>A	ENSP00000389119.1:p.Thr1146=
ENST00000468795.1:c.353C>A
NM_000492.3:c.3528C>A , LRG_663t1:c.3528C>A	NP_000483.3:p.Thr1176=
XM_011515751.1:c.3618C>A	XP_011514053.1:p.Thr1206=
XM_011515752.1:c.3618C>A	XP_011514054.1:p.Thr1206=
XM_011515753.1:c.3285C>A	XP_011514055.1:p.Thr1095=
XM_011515754.1:c.3285C>A	XP_011514056.1:p.Thr1095=
NM_000492.4:c.3528C>A MANE Select	NP_000483.3:p.Thr1176=