Canonical Allele Identifier: CA368993326

Gene: CFTR

Linked Data

• dbSNP Id: rs1178896499
• MyVariant Identifiers: chr7:g.117254682G>A (hg19) ; chr7:g.117614628G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117614628G>A , CM000669.2:g.117614628G>A	GRCh38
NC_000007.13:g.117254682G>A , CM000669.1:g.117254682G>A	GRCh37
NC_000007.12:g.117041918G>A	NCBI36
NG_016465.4:g.153845G>A , LRG_663:g.153845G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3383G>A	ENSP00000497673.2:p.Arg1128Lys
ENST00000647978.2:c.*3097G>A	ENSP00000497658.1:n.*3097G>A
ENST00000649781.2:c.3200G>A	ENSP00000497203.1:p.Arg1067Lys
ENST00000685018.2:c.3383G>A	ENSP00000510194.2:p.Arg1128Lys
ENST00000687278.2:c.3383G>A	ENSP00000509593.2:p.Arg1128Lys
ENST00000699585.1:c.3383G>A	ENSP00000514456.1:p.Arg1128Lys
ENST00000699598.1:c.3383G>A	ENSP00000514467.1:p.Arg1128Lys
ENST00000699599.1:c.3383G>A	ENSP00000514468.1:p.Arg1128Lys
ENST00000699600.1:c.3383G>A	ENSP00000514469.1:p.Arg1128Lys
ENST00000699601.1:c.*1758G>A	ENSP00000514470.1:n.*1758G>A
ENST00000699602.1:c.3377G>A	ENSP00000514471.1:p.Arg1126Lys
ENST00000699604.1:c.*3207G>A	ENSP00000514472.1:n.*3207G>A
ENST00000699605.1:c.2957G>A	ENSP00000514473.1:p.Arg986Lys
ENST00000685018.1:c.131G>A	ENSP00000510194.1:p.Arg44Lys
ENST00000687278.1:c.974G>A	ENSP00000509593.1:p.Arg325Lys
ENST00000003084.11:c.3383G>A MANE Select	ENSP00000003084.6:p.Arg1128Lys
ENST00000647720.1:c.1033G>A
ENST00000648260.1:c.2165G>A	ENSP00000497957.1:p.Arg722Lys
ENST00000649406.1:c.3200G>A	ENSP00000497965.1:p.Arg1067Lys
ENST00000649781.1:c.3200G>A	ENSP00000497203.1:p.Arg1067Lys
ENST00000003084.10:c.3383G>A	ENSP00000003084.6:p.Arg1128Lys
ENST00000426809.5:c.3293G>A	ENSP00000389119.1:p.Arg1098Lys
ENST00000468795.1:c.208G>A
NM_000492.3:c.3383G>A , LRG_663t1:c.3383G>A	NP_000483.3:p.Arg1128Lys
XM_011515751.1:c.3473G>A	XP_011514053.1:p.Arg1158Lys
XM_011515752.1:c.3473G>A	XP_011514054.1:p.Arg1158Lys
XM_011515753.1:c.3140G>A	XP_011514055.1:p.Arg1047Lys
XM_011515754.1:c.3140G>A	XP_011514056.1:p.Arg1047Lys
NM_000492.4:c.3383G>A MANE Select	NP_000483.3:p.Arg1128Lys