Canonical Allele Identifier: CA2189602576

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617051C= , CM000677.2:g.78617051C=	GRCh38
NC_000015.9:g.78909393C= , CM000677.1:g.78909393C=	GRCh37
NC_000015.8:g.76696448C=	NCBI36
NG_016143.1:g.9245G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.350G= MANE Select	ENSP00000315602.5:p.Trp117=
ENST00000326828.5:c.350G=	ENSP00000315602.5:p.Trp117=
ENST00000348639.7:c.350G=	ENSP00000267951.4:p.Trp117=
ENST00000559658.5:c.350G=	ENSP00000452896.1:p.Trp117=
NM_000743.4:c.350G=	NP_000734.2:p.Trp117=
NM_001166694.1:c.350G=	NP_001160166.1:p.Trp117=
NR_046313.1:n.851G=
XM_006720382.1:c.149G=	XP_006720445.1:p.Trp50=
XM_011521173.1:c.269G=	XP_011519475.1:p.Trp90=
XM_006720382.3:c.149G=	XP_006720445.1:p.Trp50=
NM_000743.5:c.350G= MANE Select	NP_000734.2:p.Trp117=
NM_001166694.2:c.350G=	NP_001160166.1:p.Trp117=
NR_046313.2:n.552G=