Canonical Allele Identifier: CA368996426

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117267673A>G (hg19) ; chr7:g.117627619A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117627619A>G , CM000669.2:g.117627619A>G	GRCh38
NC_000007.13:g.117267673A>G , CM000669.1:g.117267673A>G	GRCh37
NC_000007.12:g.117054909A>G	NCBI36
NG_016465.4:g.166836A>G , LRG_663:g.166836A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3517+49A>G	ENSP00000497673.2:n.3517+49A>G
ENST00000647978.2:c.*3280A>G	ENSP00000497658.1:n.*3280A>G
ENST00000649781.2:c.3383A>G	ENSP00000497203.1:p.Lys1128Arg
ENST00000685018.2:c.3566A>G	ENSP00000510194.2:p.Lys1189Arg
ENST00000687278.2:c.*219A>G	ENSP00000509593.2:n.*219A>G
ENST00000699585.1:c.3517+49A>G	ENSP00000514456.1:n.3517+49A>G
ENST00000699598.1:c.3566A>G	ENSP00000514467.1:p.Lys1189Arg
ENST00000699599.1:c.3566A>G	ENSP00000514468.1:p.Lys1189Arg
ENST00000699600.1:c.*227A>G	ENSP00000514469.1:n.*227A>G
ENST00000699601.1:c.*1941A>G	ENSP00000514470.1:n.*1941A>G
ENST00000699602.1:c.3560A>G	ENSP00000514471.1:p.Lys1187Arg
ENST00000699604.1:c.*3390A>G	ENSP00000514472.1:n.*3390A>G
ENST00000699605.1:c.3140A>G	ENSP00000514473.1:p.Lys1047Arg
ENST00000685018.1:c.314A>G	ENSP00000510194.1:p.Lys105Arg
ENST00000687278.1:c.1353A>G	ENSP00000509593.1:n.1353A>G
ENST00000689011.1:c.148A>G
ENST00000003084.11:c.3566A>G MANE Select	ENSP00000003084.6:p.Lys1189Arg
ENST00000647720.1:c.1167+49A>G
ENST00000648260.1:c.2348A>G	ENSP00000497957.1:p.Lys783Arg
ENST00000649406.1:c.3383A>G	ENSP00000497965.1:p.Lys1128Arg
ENST00000649781.1:c.3383A>G	ENSP00000497203.1:p.Lys1128Arg
ENST00000003084.10:c.3566A>G	ENSP00000003084.6:p.Lys1189Arg
ENST00000426809.5:c.3476A>G	ENSP00000389119.1:p.Lys1159Arg
ENST00000468795.1:c.391A>G
NM_000492.3:c.3566A>G , LRG_663t1:c.3566A>G	NP_000483.3:p.Lys1189Arg
XM_011515751.1:c.3656A>G	XP_011514053.1:p.Lys1219Arg
XM_011515752.1:c.3656A>G	XP_011514054.1:p.Lys1219Arg
XM_011515753.1:c.3323A>G	XP_011514055.1:p.Lys1108Arg
XM_011515754.1:c.3323A>G	XP_011514056.1:p.Lys1108Arg
NM_000492.4:c.3566A>G MANE Select	NP_000483.3:p.Lys1189Arg