Canonical Allele Identifier: CA2189590169

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601920G= , CM000677.2:g.78601920G=	GRCh38
NC_000015.9:g.78894262G= , CM000677.1:g.78894262G=	GRCh37
NC_000015.8:g.76681317G=	NCBI36
NG_016143.1:g.24376C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.722C= MANE Select	ENSP00000315602.5:p.Pro241=
ENST00000326828.5:c.722C=	ENSP00000315602.5:p.Pro241=
ENST00000348639.7:c.722C=	ENSP00000267951.4:p.Pro241=
ENST00000558903.1:n.429C=
ENST00000559658.5:c.722C=	ENSP00000452896.1:p.Pro241=
NM_000743.4:c.722C=	NP_000734.2:p.Pro241=
NM_001166694.1:c.722C=	NP_001160166.1:p.Pro241=
NR_046313.1:n.1223C=
XM_006720382.1:c.521C=	XP_006720445.1:p.Pro174=
XM_011521173.1:c.641C=	XP_011519475.1:p.Pro214=
XM_006720382.3:c.521C=	XP_006720445.1:p.Pro174=
NM_000743.5:c.722C= MANE Select	NP_000734.2:p.Pro241=
NM_001166694.2:c.722C=	NP_001160166.1:p.Pro241=
NR_046313.2:n.924C=