Canonical Allele Identifier: CA971782846

Gene: CHRNA3

Linked Data

• gnomAD v3: 15-78601981-A-AT
• gnomAD v4: 15-78601981-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601981_78601982insT , CM000677.2:g.78601981_78601982insT	GRCh38
NC_000015.9:g.78894323_78894324insT , CM000677.1:g.78894323_78894324insT	GRCh37
NC_000015.8:g.76681378_76681379insT	NCBI36
NG_016143.1:g.24314_24315insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.660_661insA MANE Select	ENSP00000315602.5:p.Tyr221IlefsTer?
ENST00000326828.5:c.660_661insA	ENSP00000315602.5:p.Tyr221IlefsTer?
ENST00000348639.7:c.660_661insA	ENSP00000267951.4:p.Tyr221IlefsTer?
ENST00000558903.1:n.367_368insA
ENST00000559658.5:c.660_661insA	ENSP00000452896.1:p.Tyr221IlefsTer?
NM_000743.4:c.660_661insA	NP_000734.2:p.Tyr221IlefsTer?
NM_001166694.1:c.660_661insA	NP_001160166.1:p.Tyr221IlefsTer?
NR_046313.1:n.1161_1162insA
XM_006720382.1:c.459_460insA	XP_006720445.1:p.Tyr154IlefsTer?
XM_011521173.1:c.579_580insA	XP_011519475.1:p.Tyr194IlefsTer?
XM_006720382.3:c.459_460insA	XP_006720445.1:p.Tyr154IlefsTer?
NM_000743.5:c.660_661insA MANE Select	NP_000734.2:p.Tyr221IlefsTer?
NM_001166694.2:c.660_661insA	NP_001160166.1:p.Tyr221IlefsTer?
NR_046313.2:n.862_863insA