Canonical Allele Identifier: CA457228874

Gene: CFTR CFTR-AS1

Linked Data

• MyVariant Identifiers: chr7:g.117199655T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117559601T>C , CM000669.2:g.117559601T>C	GRCh38
NC_000007.13:g.117199655T>C , CM000669.1:g.117199655T>C	GRCh37
NC_000007.12:g.116986891T>C	NCBI36
NG_016465.4:g.98818T>C , LRG_663:g.98818T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.1530T>C (CFTR)	ENSP00000497673.2:p.Val510=
ENST00000647978.2:c.*1244T>C (CFTR)	ENSP00000497658.1:n.*1244T>C
ENST00000649781.2:c.1347T>C (CFTR)	ENSP00000497203.1:p.Val449=
ENST00000685018.2:c.1530T>C (CFTR)	ENSP00000510194.2:p.Val510=
ENST00000687278.2:c.1530T>C (CFTR)	ENSP00000509593.2:p.Val510=
ENST00000699585.1:c.1530T>C (CFTR)	ENSP00000514456.1:p.Val510=
ENST00000699596.1:c.1530T>C (CFTR)	ENSP00000514465.1:p.Val510=
ENST00000699597.1:c.*88T>C (CFTR)	ENSP00000514466.1:n.*88T>C
ENST00000699598.1:c.1530T>C (CFTR)	ENSP00000514467.1:p.Val510=
ENST00000699599.1:c.1530T>C (CFTR)	ENSP00000514468.1:p.Val510=
ENST00000699600.1:c.1530T>C (CFTR)	ENSP00000514469.1:p.Val510=
ENST00000699601.1:c.1530T>C (CFTR)	ENSP00000514470.1:p.Val510=
ENST00000699602.1:c.1530T>C (CFTR)	ENSP00000514471.1:p.Val510=
ENST00000699604.1:c.*1354T>C (CFTR)	ENSP00000514472.1:n.*1354T>C
ENST00000699605.1:c.1104T>C (CFTR)	ENSP00000514473.1:p.Val368=
ENST00000003084.11:c.1530T>C (CFTR) MANE Select	ENSP00000003084.6:p.Val510=
ENST00000647978.1:c.*1244T>C (CFTR)	ENSP00000497658.1:n.*1244T>C
ENST00000648260.1:c.1347T>C (CFTR)	ENSP00000497957.1:p.Val449=
ENST00000649406.1:c.1347T>C (CFTR)	ENSP00000497965.1:p.Val449=
ENST00000649781.1:c.1347T>C (CFTR)	ENSP00000497203.1:p.Val449=
ENST00000003084.10:c.1530T>C (CFTR)	ENSP00000003084.6:p.Val510=
ENST00000426809.5:c.1440T>C (CFTR)	ENSP00000389119.1:p.Val480=
NM_000492.3:c.1530T>C , LRG_663t1:c.1530T>C (CFTR)	NP_000483.3:p.Val510=
XM_011515751.1:c.1620T>C (CFTR)	XP_011514053.1:p.Val540=
XM_011515752.1:c.1620T>C (CFTR)	XP_011514054.1:p.Val540=
XM_011515753.1:c.1287T>C (CFTR)	XP_011514055.1:p.Val429=
XM_011515754.1:c.1287T>C (CFTR)	XP_011514056.1:p.Val429=
NR_149084.1:n.221+1132A>G (CFTR-AS1)
NM_000492.4:c.1530T>C (CFTR) MANE Select	NP_000483.3:p.Val510=