Canonical Allele Identifier: CA2189590014

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601868G= , CM000677.2:g.78601868G=	GRCh38
NC_000015.9:g.78894210G= , CM000677.1:g.78894210G=	GRCh37
NC_000015.8:g.76681265G=	NCBI36
NG_016143.1:g.24428C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.774C= MANE Select	ENSP00000315602.5:p.Leu258=
ENST00000326828.5:c.774C=	ENSP00000315602.5:p.Leu258=
ENST00000348639.7:c.774C=	ENSP00000267951.4:p.Leu258=
ENST00000558903.1:n.481C=
ENST00000559658.5:c.774C=	ENSP00000452896.1:p.Leu258=
NM_000743.4:c.774C=	NP_000734.2:p.Leu258=
NM_001166694.1:c.774C=	NP_001160166.1:p.Leu258=
NR_046313.1:n.1275C=
XM_006720382.1:c.573C=	XP_006720445.1:p.Leu191=
XM_011521173.1:c.693C=	XP_011519475.1:p.Leu231=
XM_006720382.3:c.573C=	XP_006720445.1:p.Leu191=
NM_000743.5:c.774C= MANE Select	NP_000734.2:p.Leu258=
NM_001166694.2:c.774C=	NP_001160166.1:p.Leu258=
NR_046313.2:n.976C=