Canonical Allele Identifier: CA368997389

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117267770A>C (hg19) ; chr7:g.117627716A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117627716A>C , CM000669.2:g.117627716A>C	GRCh38
NC_000007.13:g.117267770A>C , CM000669.1:g.117267770A>C	GRCh37
NC_000007.12:g.117055006A>C	NCBI36
NG_016465.4:g.166933A>C , LRG_663:g.166933A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3517+146A>C	ENSP00000497673.2:n.3517+146A>C
ENST00000647978.2:c.*3377A>C	ENSP00000497658.1:n.*3377A>C
ENST00000649781.2:c.3480A>C	ENSP00000497203.1:p.Glu1160Asp
ENST00000685018.2:c.3663A>C	ENSP00000510194.2:p.Glu1221Asp
ENST00000687278.2:c.*316A>C	ENSP00000509593.2:n.*316A>C
ENST00000699585.1:c.3517+146A>C	ENSP00000514456.1:n.3517+146A>C
ENST00000699598.1:c.3663A>C	ENSP00000514467.1:p.Glu1221Asp
ENST00000699599.1:c.3663A>C	ENSP00000514468.1:p.Glu1221Asp
ENST00000699600.1:c.*324A>C	ENSP00000514469.1:n.*324A>C
ENST00000699601.1:c.*2038A>C	ENSP00000514470.1:n.*2038A>C
ENST00000699602.1:c.3657A>C	ENSP00000514471.1:p.Glu1219Asp
ENST00000699604.1:c.*3487A>C	ENSP00000514472.1:n.*3487A>C
ENST00000699605.1:c.3237A>C	ENSP00000514473.1:p.Glu1079Asp
ENST00000685018.1:c.411A>C	ENSP00000510194.1:p.Glu137Asp
ENST00000687278.1:c.1450A>C	ENSP00000509593.1:n.1450A>C
ENST00000689011.1:c.245A>C
ENST00000003084.11:c.3663A>C MANE Select	ENSP00000003084.6:p.Glu1221Asp
ENST00000647720.1:c.1167+146A>C
ENST00000648260.1:c.2445A>C	ENSP00000497957.1:p.Glu815Asp
ENST00000649406.1:c.3480A>C	ENSP00000497965.1:p.Glu1160Asp
ENST00000649781.1:c.3480A>C	ENSP00000497203.1:p.Glu1160Asp
ENST00000003084.10:c.3663A>C	ENSP00000003084.6:p.Glu1221Asp
ENST00000426809.5:c.3573A>C	ENSP00000389119.1:p.Glu1191Asp
ENST00000468795.1:c.488A>C
NM_000492.3:c.3663A>C , LRG_663t1:c.3663A>C	NP_000483.3:p.Glu1221Asp
XM_011515751.1:c.3753A>C	XP_011514053.1:p.Glu1251Asp
XM_011515752.1:c.3753A>C	XP_011514054.1:p.Glu1251Asp
XM_011515753.1:c.3420A>C	XP_011514055.1:p.Glu1140Asp
XM_011515754.1:c.3420A>C	XP_011514056.1:p.Glu1140Asp
NM_000492.4:c.3663A>C MANE Select	NP_000483.3:p.Glu1221Asp