Canonical Allele Identifier: CA457231140

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117267581A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117627527A>C , CM000669.2:g.117627527A>C	GRCh38
NC_000007.13:g.117267581A>C , CM000669.1:g.117267581A>C	GRCh37
NC_000007.12:g.117054817A>C	NCBI36
NG_016465.4:g.166744A>C , LRG_663:g.166744A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3474A>C	ENSP00000497673.2:p.Arg1158=
ENST00000647978.2:c.*3188A>C	ENSP00000497658.1:n.*3188A>C
ENST00000649781.2:c.3291A>C	ENSP00000497203.1:p.Arg1097=
ENST00000685018.2:c.3474A>C	ENSP00000510194.2:p.Arg1158=
ENST00000687278.2:c.*127A>C	ENSP00000509593.2:n.*127A>C
ENST00000699585.1:c.3474A>C	ENSP00000514456.1:p.Arg1158=
ENST00000699598.1:c.3474A>C	ENSP00000514467.1:p.Arg1158=
ENST00000699599.1:c.3474A>C	ENSP00000514468.1:p.Arg1158=
ENST00000699600.1:c.*135A>C	ENSP00000514469.1:n.*135A>C
ENST00000699601.1:c.*1849A>C	ENSP00000514470.1:n.*1849A>C
ENST00000699602.1:c.3468A>C	ENSP00000514471.1:p.Arg1156=
ENST00000699604.1:c.*3298A>C	ENSP00000514472.1:n.*3298A>C
ENST00000699605.1:c.3048A>C	ENSP00000514473.1:p.Arg1016=
ENST00000685018.1:c.222A>C	ENSP00000510194.1:p.Arg74=
ENST00000687278.1:c.1261A>C	ENSP00000509593.1:n.1261A>C
ENST00000689011.1:c.56A>C
ENST00000003084.11:c.3474A>C MANE Select	ENSP00000003084.6:p.Arg1158=
ENST00000647720.1:c.1124A>C
ENST00000648260.1:c.2256A>C	ENSP00000497957.1:p.Arg752=
ENST00000649406.1:c.3291A>C	ENSP00000497965.1:p.Arg1097=
ENST00000649781.1:c.3291A>C	ENSP00000497203.1:p.Arg1097=
ENST00000003084.10:c.3474A>C	ENSP00000003084.6:p.Arg1158=
ENST00000426809.5:c.3384A>C	ENSP00000389119.1:p.Arg1128=
ENST00000468795.1:c.299A>C
NM_000492.3:c.3474A>C , LRG_663t1:c.3474A>C	NP_000483.3:p.Arg1158=
XM_011515751.1:c.3564A>C	XP_011514053.1:p.Arg1188=
XM_011515752.1:c.3564A>C	XP_011514054.1:p.Arg1188=
XM_011515753.1:c.3231A>C	XP_011514055.1:p.Arg1077=
XM_011515754.1:c.3231A>C	XP_011514056.1:p.Arg1077=
NM_000492.4:c.3474A>C MANE Select	NP_000483.3:p.Arg1158=