Canonical Allele Identifier: CA920252041

Gene: CHRNA4

Linked Data

• dbSNP Id: rs1555837882

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350540_63350541insAGC , CM000682.2:g.63350540_63350541insAGC	GRCh38
NC_000020.10:g.61981892_61981893insAGC , CM000682.1:g.61981892_61981893insAGC	GRCh37
NC_000020.9:g.61452336_61452337insAGC	NCBI36
NG_011931.1:g.15803_15804insGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.870_871insGCT MANE Select	ENSP00000359285.4:p.Leu290_Leu291insAla
ENST00000370263.8:c.870_871insGCT	ENSP00000359285.4:p.Leu290_Leu291insAla
ENST00000463705.5:n.1518_1519insGCT
ENST00000467563.3:n.940_941insGCT
ENST00000498043.6:c.894_895insGCT
ENST00000615287.4:c.657_658insGCT	ENSP00000483388.1:p.Leu219_Leu220insAla
ENST00000627000.1:c.*559_*560insGCT	ENSP00000486914.1:n.*559_*560insGCT
ENST00000630240.1:n.591_592insGCT
NM_000744.6:c.870_871insGCT	NP_000735.1:p.Leu290_Leu291insAla
NM_001256573.1:c.342_343insGCT	NP_001243502.1:p.Leu114_Leu115insAla
NR_046317.1:n.1126_1127insGCT
XM_011528524.1:c.657_658insGCT	XP_011526826.1:p.Leu219_Leu220insAla
XM_017027625.2:c.342_343insGCT	XP_016883114.1:p.Leu114_Leu115insAla
XM_024451822.1:c.342_343insGCT	XP_024307590.1:p.Leu114_Leu115insAla
NM_001256573.2:c.342_343insGCT	NP_001243502.1:p.Leu114_Leu115insAla
NR_046317.2:n.1079_1080insGCT
NM_000744.7:c.870_871insGCT MANE Select	NP_000735.1:p.Leu290_Leu291insAla