Canonical Allele Identifier: CA2189590152

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601916C= , CM000677.2:g.78601916C=	GRCh38
NC_000015.9:g.78894258C= , CM000677.1:g.78894258C=	GRCh37
NC_000015.8:g.76681313C=	NCBI36
NG_016143.1:g.24380G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.726G= MANE Select	ENSP00000315602.5:p.Leu242=
ENST00000326828.5:c.726G=	ENSP00000315602.5:p.Leu242=
ENST00000348639.7:c.726G=	ENSP00000267951.4:p.Leu242=
ENST00000558903.1:n.433G=
ENST00000559658.5:c.726G=	ENSP00000452896.1:p.Leu242=
NM_000743.4:c.726G=	NP_000734.2:p.Leu242=
NM_001166694.1:c.726G=	NP_001160166.1:p.Leu242=
NR_046313.1:n.1227G=
XM_006720382.1:c.525G=	XP_006720445.1:p.Leu175=
XM_011521173.1:c.645G=	XP_011519475.1:p.Leu215=
XM_006720382.3:c.525G=	XP_006720445.1:p.Leu175=
NM_000743.5:c.726G= MANE Select	NP_000734.2:p.Leu242=
NM_001166694.2:c.726G=	NP_001160166.1:p.Leu242=
NR_046313.2:n.928G=