Canonical Allele Identifier: CA2189590080

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601887C= , CM000677.2:g.78601887C=	GRCh38
NC_000015.9:g.78894229C= , CM000677.1:g.78894229C=	GRCh37
NC_000015.8:g.76681284C=	NCBI36
NG_016143.1:g.24409G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.755G= MANE Select	ENSP00000315602.5:p.Cys252=
ENST00000326828.5:c.755G=	ENSP00000315602.5:p.Cys252=
ENST00000348639.7:c.755G=	ENSP00000267951.4:p.Cys252=
ENST00000558903.1:n.462G=
ENST00000559658.5:c.755G=	ENSP00000452896.1:p.Cys252=
NM_000743.4:c.755G=	NP_000734.2:p.Cys252=
NM_001166694.1:c.755G=	NP_001160166.1:p.Cys252=
NR_046313.1:n.1256G=
XM_006720382.1:c.554G=	XP_006720445.1:p.Cys185=
XM_011521173.1:c.674G=	XP_011519475.1:p.Cys225=
XM_006720382.3:c.554G=	XP_006720445.1:p.Cys185=
NM_000743.5:c.755G= MANE Select	NP_000734.2:p.Cys252=
NM_001166694.2:c.755G=	NP_001160166.1:p.Cys252=
NR_046313.2:n.957G=