Canonical Allele Identifier: CA393585727

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894395T>A (hg19) ; chr15:g.78602053T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602053T>A , CM000677.2:g.78602053T>A	GRCh38
NC_000015.9:g.78894395T>A , CM000677.1:g.78894395T>A	GRCh37
NC_000015.8:g.76681450T>A	NCBI36
NG_016143.1:g.24243A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.589A>T MANE Select	ENSP00000315602.5:p.Asn197Tyr
ENST00000326828.5:c.589A>T	ENSP00000315602.5:p.Asn197Tyr
ENST00000348639.7:c.589A>T	ENSP00000267951.4:p.Asn197Tyr
ENST00000558903.1:n.296A>T
ENST00000559658.5:c.589A>T	ENSP00000452896.1:p.Asn197Tyr
NM_000743.4:c.589A>T	NP_000734.2:p.Asn197Tyr
NM_001166694.1:c.589A>T	NP_001160166.1:p.Asn197Tyr
NR_046313.1:n.1090A>T
XM_006720382.1:c.388A>T	XP_006720445.1:p.Asn130Tyr
XM_011521173.1:c.508A>T	XP_011519475.1:p.Asn170Tyr
XM_006720382.3:c.388A>T	XP_006720445.1:p.Asn130Tyr
NM_000743.5:c.589A>T MANE Select	NP_000734.2:p.Asn197Tyr
NM_001166694.2:c.589A>T	NP_001160166.1:p.Asn197Tyr
NR_046313.2:n.791A>T