Canonical Allele Identifier: CA7684233

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78596663A>T , CM000677.2:g.78596663A>T	GRCh38
NC_000015.9:g.78889005A>T , CM000677.1:g.78889005A>T	GRCh37
NC_000015.8:g.76676060A>T	NCBI36
NG_016143.1:g.29633T>A
NG_023328.1:g.36144A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000743.5:c.1459T>A MANE Select	NP_000734.2:p.Cys487Ser
ENST00000326828.6:c.1459T>A MANE Select	ENSP00000315602.5:p.Cys487Ser
NM_000743.4:c.1459T>A	NP_000734.2:p.Cys487Ser
NM_001166694.1:c.1390-3472T>A	NP_001160166.1:n.1390-3472T>A
NM_001166694.2:c.1390-3472T>A	NP_001160166.1:n.1390-3472T>A
NR_046313.1:n.1960T>A
NR_046313.2:n.1661T>A
ENST00000326828.5:c.1459T>A	ENSP00000315602.5:p.Cys487Ser
ENST00000348639.7:c.1390-3472T>A	ENSP00000267951.4:n.1390-3472T>A
ENST00000559002.5:n.70T>A
ENST00000559658.5:c.1459T>A	ENSP00000452896.1:p.Cys487Ser
XM_006720382.1:c.1258T>A	XP_006720445.1:p.Cys420Ser
XM_006720382.3:c.1258T>A	XP_006720445.1:p.Cys420Ser
XM_011521173.1:c.1378T>A	XP_011519475.1:p.Cys460Ser