Canonical Allele Identifier: CA7684296

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601399A>C , CM000677.2:g.78601399A>C	GRCh38
NC_000015.9:g.78893741A>C , CM000677.1:g.78893741A>C	GRCh37
NC_000015.8:g.76680796A>C	NCBI36
NG_016143.1:g.24897T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.1243T>G MANE Select	ENSP00000315602.5:p.Phe415Val
ENST00000326828.5:c.1243T>G	ENSP00000315602.5:p.Phe415Val
ENST00000348639.7:c.1243T>G	ENSP00000267951.4:p.Phe415Val
ENST00000559658.5:c.1243T>G	ENSP00000452896.1:p.Phe415Val
NM_000743.4:c.1243T>G	NP_000734.2:p.Phe415Val
NM_001166694.1:c.1243T>G	NP_001160166.1:p.Phe415Val
NR_046313.1:n.1744T>G
XM_006720382.1:c.1042T>G	XP_006720445.1:p.Phe348Val
XM_011521173.1:c.1162T>G	XP_011519475.1:p.Phe388Val
XM_006720382.3:c.1042T>G	XP_006720445.1:p.Phe348Val
NM_000743.5:c.1243T>G MANE Select	NP_000734.2:p.Phe415Val
NM_001166694.2:c.1243T>G	NP_001160166.1:p.Phe415Val
NR_046313.2:n.1445T>G