Canonical Allele Identifier: CA2189589941

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601837A= , CM000677.2:g.78601837A=	GRCh38
NC_000015.9:g.78894179A= , CM000677.1:g.78894179A=	GRCh37
NC_000015.8:g.76681234A=	NCBI36
NG_016143.1:g.24459T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.805T= MANE Select	ENSP00000315602.5:p.Cys269=
ENST00000326828.5:c.805T=	ENSP00000315602.5:p.Cys269=
ENST00000348639.7:c.805T=	ENSP00000267951.4:p.Cys269=
ENST00000558903.1:n.512T=
ENST00000559658.5:c.805T=	ENSP00000452896.1:p.Cys269=
NM_000743.4:c.805T=	NP_000734.2:p.Cys269=
NM_001166694.1:c.805T=	NP_001160166.1:p.Cys269=
NR_046313.1:n.1306T=
XM_006720382.1:c.604T=	XP_006720445.1:p.Cys202=
XM_011521173.1:c.724T=	XP_011519475.1:p.Cys242=
XM_006720382.3:c.604T=	XP_006720445.1:p.Cys202=
NM_000743.5:c.805T= MANE Select	NP_000734.2:p.Cys269=
NM_001166694.2:c.805T=	NP_001160166.1:p.Cys269=
NR_046313.2:n.1007T=