Canonical Allele Identifier: CA2189590367

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601971_78601973delinsCAG , CM000677.2:g.78601971_78601973delinsCAG	GRCh38
NC_000015.9:g.78894313_78894315delinsCAG , CM000677.1:g.78894313_78894315delinsCAG	GRCh37
NC_000015.8:g.76681368_76681370delinsCAG	NCBI36
NG_016143.1:g.24323_24325delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.669_671delinsCTG MANE Select	ENSP00000315602.5:p.Cys223=
ENST00000326828.5:c.669_671delinsCTG	ENSP00000315602.5:p.Cys223=
ENST00000348639.7:c.669_671delinsCTG	ENSP00000267951.4:p.Cys223=
ENST00000558903.1:n.376_378delinsCTG
ENST00000559658.5:c.669_671delinsCTG	ENSP00000452896.1:p.Cys223=
NM_000743.4:c.669_671delinsCTG	NP_000734.2:p.Cys223=
NM_001166694.1:c.669_671delinsCTG	NP_001160166.1:p.Cys223=
NR_046313.1:n.1170_1172delinsCTG
XM_006720382.1:c.468_470delinsCTG	XP_006720445.1:p.Cys156=
XM_011521173.1:c.588_590delinsCTG	XP_011519475.1:p.Cys196=
XM_006720382.3:c.468_470delinsCTG	XP_006720445.1:p.Cys156=
NM_000743.5:c.669_671delinsCTG MANE Select	NP_000734.2:p.Cys223=
NM_001166694.2:c.669_671delinsCTG	NP_001160166.1:p.Cys223=
NR_046313.2:n.871_873delinsCTG