Canonical Allele Identifier: CA393585599

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894352T>A (hg19) ; chr15:g.78602010T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602010T>A , CM000677.2:g.78602010T>A	GRCh38
NC_000015.9:g.78894352T>A , CM000677.1:g.78894352T>A	GRCh37
NC_000015.8:g.76681407T>A	NCBI36
NG_016143.1:g.24286A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.632A>T MANE Select	ENSP00000315602.5:p.Lys211Ile
ENST00000326828.5:c.632A>T	ENSP00000315602.5:p.Lys211Ile
ENST00000348639.7:c.632A>T	ENSP00000267951.4:p.Lys211Ile
ENST00000558903.1:n.339A>T
ENST00000559658.5:c.632A>T	ENSP00000452896.1:p.Lys211Ile
NM_000743.4:c.632A>T	NP_000734.2:p.Lys211Ile
NM_001166694.1:c.632A>T	NP_001160166.1:p.Lys211Ile
NR_046313.1:n.1133A>T
XM_006720382.1:c.431A>T	XP_006720445.1:p.Lys144Ile
XM_011521173.1:c.551A>T	XP_011519475.1:p.Lys184Ile
XM_006720382.3:c.431A>T	XP_006720445.1:p.Lys144Ile
NM_000743.5:c.632A>T MANE Select	NP_000734.2:p.Lys211Ile
NM_001166694.2:c.632A>T	NP_001160166.1:p.Lys211Ile
NR_046313.2:n.834A>T