Canonical Allele Identifier: CA7684375

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601685G>A , CM000677.2:g.78601685G>A	GRCh38
NC_000015.9:g.78894027G>A , CM000677.1:g.78894027G>A	GRCh37
NC_000015.8:g.76681082G>A	NCBI36
NG_016143.1:g.24611C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000743.5:c.957C>T MANE Select	NP_000734.2:p.Ile319=
ENST00000326828.6:c.957C>T MANE Select	ENSP00000315602.5:p.Ile319=
NM_000743.4:c.957C>T	NP_000734.2:p.Ile319=
NM_001166694.1:c.957C>T	NP_001160166.1:p.Ile319=
NM_001166694.2:c.957C>T	NP_001160166.1:p.Ile319=
NR_046313.1:n.1458C>T
NR_046313.2:n.1159C>T
ENST00000326828.5:c.957C>T	ENSP00000315602.5:p.Ile319=
ENST00000348639.7:c.957C>T	ENSP00000267951.4:p.Ile319=
ENST00000559658.5:c.957C>T	ENSP00000452896.1:p.Ile319=
XM_006720382.1:c.756C>T	XP_006720445.1:p.Ile252=
XM_006720382.3:c.756C>T	XP_006720445.1:p.Ile252=
XM_011521173.1:c.876C>T	XP_011519475.1:p.Ile292=