Canonical Allele Identifier: CA2189590054

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601879T= , CM000677.2:g.78601879T=	GRCh38
NC_000015.9:g.78894221T= , CM000677.1:g.78894221T=	GRCh37
NC_000015.8:g.76681276T=	NCBI36
NG_016143.1:g.24417A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.763A= MANE Select	ENSP00000315602.5:p.Ile255=
ENST00000326828.5:c.763A=	ENSP00000315602.5:p.Ile255=
ENST00000348639.7:c.763A=	ENSP00000267951.4:p.Ile255=
ENST00000558903.1:n.470A=
ENST00000559658.5:c.763A=	ENSP00000452896.1:p.Ile255=
NM_000743.4:c.763A=	NP_000734.2:p.Ile255=
NM_001166694.1:c.763A=	NP_001160166.1:p.Ile255=
NR_046313.1:n.1264A=
XM_006720382.1:c.562A=	XP_006720445.1:p.Ile188=
XM_011521173.1:c.682A=	XP_011519475.1:p.Ile228=
XM_006720382.3:c.562A=	XP_006720445.1:p.Ile188=
NM_000743.5:c.763A= MANE Select	NP_000734.2:p.Ile255=
NM_001166694.2:c.763A=	NP_001160166.1:p.Ile255=
NR_046313.2:n.965A=