Canonical Allele Identifier: CA457228778

Gene: CFTR CFTR-AS1

Linked Data

• MyVariant Identifiers: chr7:g.117199584A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117559530A>C , CM000669.2:g.117559530A>C	GRCh38
NC_000007.13:g.117199584A>C , CM000669.1:g.117199584A>C	GRCh37
NC_000007.12:g.116986820A>C	NCBI36
NG_016465.4:g.98747A>C , LRG_663:g.98747A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.1459A>C (CFTR)	ENSP00000497673.2:p.Arg487=
ENST00000647978.2:c.*1173A>C (CFTR)	ENSP00000497658.1:n.*1173A>C
ENST00000649781.2:c.1276A>C (CFTR)	ENSP00000497203.1:p.Arg426=
ENST00000685018.2:c.1459A>C (CFTR)	ENSP00000510194.2:p.Arg487=
ENST00000687278.2:c.1459A>C (CFTR)	ENSP00000509593.2:p.Arg487=
ENST00000699585.1:c.1459A>C (CFTR)	ENSP00000514456.1:p.Arg487=
ENST00000699596.1:c.1459A>C (CFTR)	ENSP00000514465.1:p.Arg487=
ENST00000699597.1:c.*17A>C (CFTR)	ENSP00000514466.1:n.*17A>C
ENST00000699598.1:c.1459A>C (CFTR)	ENSP00000514467.1:p.Arg487=
ENST00000699599.1:c.1459A>C (CFTR)	ENSP00000514468.1:p.Arg487=
ENST00000699600.1:c.1459A>C (CFTR)	ENSP00000514469.1:p.Arg487=
ENST00000699601.1:c.1459A>C (CFTR)	ENSP00000514470.1:p.Arg487=
ENST00000699602.1:c.1459A>C (CFTR)	ENSP00000514471.1:p.Arg487=
ENST00000699604.1:c.*1283A>C (CFTR)	ENSP00000514472.1:n.*1283A>C
ENST00000699605.1:c.1033A>C (CFTR)	ENSP00000514473.1:p.Arg345=
ENST00000003084.11:c.1459A>C (CFTR) MANE Select	ENSP00000003084.6:p.Arg487=
ENST00000647978.1:c.*1173A>C (CFTR)	ENSP00000497658.1:n.*1173A>C
ENST00000648260.1:c.1276A>C (CFTR)	ENSP00000497957.1:p.Arg426=
ENST00000649406.1:c.1276A>C (CFTR)	ENSP00000497965.1:p.Arg426=
ENST00000649781.1:c.1276A>C (CFTR)	ENSP00000497203.1:p.Arg426=
ENST00000003084.10:c.1459A>C (CFTR)	ENSP00000003084.6:p.Arg487=
ENST00000426809.5:c.1369A>C (CFTR)	ENSP00000389119.1:p.Arg457=
NM_000492.3:c.1459A>C , LRG_663t1:c.1459A>C (CFTR)	NP_000483.3:p.Arg487=
XM_011515751.1:c.1549A>C (CFTR)	XP_011514053.1:p.Arg517=
XM_011515752.1:c.1549A>C (CFTR)	XP_011514054.1:p.Arg517=
XM_011515753.1:c.1216A>C (CFTR)	XP_011514055.1:p.Arg406=
XM_011515754.1:c.1216A>C (CFTR)	XP_011514056.1:p.Arg406=
NR_149084.1:n.221+1203T>G (CFTR-AS1)
NM_000492.4:c.1459A>C (CFTR) MANE Select	NP_000483.3:p.Arg487=