Canonical Allele Identifier: CA7684371

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601670G>A , CM000677.2:g.78601670G>A	GRCh38
NC_000015.9:g.78894012G>A , CM000677.1:g.78894012G>A	GRCh37
NC_000015.8:g.76681067G>A	NCBI36
NG_016143.1:g.24626C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000743.5:c.972C>T MANE Select	NP_000734.2:p.Phe324=
ENST00000326828.6:c.972C>T MANE Select	ENSP00000315602.5:p.Phe324=
NM_000743.4:c.972C>T	NP_000734.2:p.Phe324=
NM_001166694.1:c.972C>T	NP_001160166.1:p.Phe324=
NM_001166694.2:c.972C>T	NP_001160166.1:p.Phe324=
NR_046313.1:n.1473C>T
NR_046313.2:n.1174C>T
ENST00000326828.5:c.972C>T	ENSP00000315602.5:p.Phe324=
ENST00000348639.7:c.972C>T	ENSP00000267951.4:p.Phe324=
ENST00000559658.5:c.972C>T	ENSP00000452896.1:p.Phe324=
XM_006720382.1:c.771C>T	XP_006720445.1:p.Phe257=
XM_006720382.3:c.771C>T	XP_006720445.1:p.Phe257=
XM_011521173.1:c.891C>T	XP_011519475.1:p.Phe297=