Canonical Allele Identifier: CA2189590995

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602227C= , CM000677.2:g.78602227C=	GRCh38
NC_000015.9:g.78894569C= , CM000677.1:g.78894569C=	GRCh37
NC_000015.8:g.76681624C=	NCBI36
NG_016143.1:g.24069G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.415G= MANE Select	ENSP00000315602.5:p.Ala139=
ENST00000326828.5:c.415G=	ENSP00000315602.5:p.Ala139=
ENST00000348639.7:c.415G=	ENSP00000267951.4:p.Ala139=
ENST00000558903.1:n.122G=
ENST00000559658.5:c.415G=	ENSP00000452896.1:p.Ala139=
NM_000743.4:c.415G=	NP_000734.2:p.Ala139=
NM_001166694.1:c.415G=	NP_001160166.1:p.Ala139=
NR_046313.1:n.916G=
XM_006720382.1:c.214G=	XP_006720445.1:p.Ala72=
XM_011521173.1:c.334G=	XP_011519475.1:p.Ala112=
XM_006720382.3:c.214G=	XP_006720445.1:p.Ala72=
NM_000743.5:c.415G= MANE Select	NP_000734.2:p.Ala139=
NM_001166694.2:c.415G=	NP_001160166.1:p.Ala139=
NR_046313.2:n.617G=