Canonical Allele Identifier: CA393586337

Gene: CHRNA3

Linked Data

• MyVariant Identifiers: chr15:g.78894527C>T (hg19) ; chr15:g.78602185C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602185C>T , CM000677.2:g.78602185C>T	GRCh38
NC_000015.9:g.78894527C>T , CM000677.1:g.78894527C>T	GRCh37
NC_000015.8:g.76681582C>T	NCBI36
NG_016143.1:g.24111G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.457G>A MANE Select	ENSP00000315602.5:p.Ala153Thr
ENST00000326828.5:c.457G>A	ENSP00000315602.5:p.Ala153Thr
ENST00000348639.7:c.457G>A	ENSP00000267951.4:p.Ala153Thr
ENST00000558903.1:n.164G>A
ENST00000559658.5:c.457G>A	ENSP00000452896.1:p.Ala153Thr
NM_000743.4:c.457G>A	NP_000734.2:p.Ala153Thr
NM_001166694.1:c.457G>A	NP_001160166.1:p.Ala153Thr
NR_046313.1:n.958G>A
XM_006720382.1:c.256G>A	XP_006720445.1:p.Ala86Thr
XM_011521173.1:c.376G>A	XP_011519475.1:p.Ala126Thr
XM_006720382.3:c.256G>A	XP_006720445.1:p.Ala86Thr
NM_000743.5:c.457G>A MANE Select	NP_000734.2:p.Ala153Thr
NM_001166694.2:c.457G>A	NP_001160166.1:p.Ala153Thr
NR_046313.2:n.659G>A