Canonical Allele Identifier: CA393586456

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894546C>A (hg19) ; chr15:g.78602204C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602204C>A , CM000677.2:g.78602204C>A	GRCh38
NC_000015.9:g.78894546C>A , CM000677.1:g.78894546C>A	GRCh37
NC_000015.8:g.76681601C>A	NCBI36
NG_016143.1:g.24092G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.438G>T MANE Select	ENSP00000315602.5:p.Glu146Asp
ENST00000326828.5:c.438G>T	ENSP00000315602.5:p.Glu146Asp
ENST00000348639.7:c.438G>T	ENSP00000267951.4:p.Glu146Asp
ENST00000558903.1:n.145G>T
ENST00000559658.5:c.438G>T	ENSP00000452896.1:p.Glu146Asp
NM_000743.4:c.438G>T	NP_000734.2:p.Glu146Asp
NM_001166694.1:c.438G>T	NP_001160166.1:p.Glu146Asp
NR_046313.1:n.939G>T
XM_006720382.1:c.237G>T	XP_006720445.1:p.Glu79Asp
XM_011521173.1:c.357G>T	XP_011519475.1:p.Glu119Asp
XM_006720382.3:c.237G>T	XP_006720445.1:p.Glu79Asp
NM_000743.5:c.438G>T MANE Select	NP_000734.2:p.Glu146Asp
NM_001166694.2:c.438G>T	NP_001160166.1:p.Glu146Asp
NR_046313.2:n.640G>T