Canonical Allele Identifier: CA619417544

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1344950591
• gnomAD v2: 15-78894313-CAG-C
• gnomAD v3: 15-78601971-CAG-C
• gnomAD v4: 15-78601971-CAG-C
• MyVariant Identifiers: chr15:g.78894314_78894315del (hg19) ; chr15:g.78601972_78601973del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601972_78601973del , CM000677.2:g.78601972_78601973del	GRCh38
NC_000015.9:g.78894314_78894315del , CM000677.1:g.78894314_78894315del	GRCh37
NC_000015.8:g.76681369_76681370del	NCBI36
NG_016143.1:g.24323_24324del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.669_670del MANE Select	ENSP00000315602.5:p.Cys223TrpfsTer?
ENST00000326828.5:c.669_670del	ENSP00000315602.5:p.Cys223TrpfsTer?
ENST00000348639.7:c.669_670del	ENSP00000267951.4:p.Cys223TrpfsTer?
ENST00000558903.1:n.376_377del
ENST00000559658.5:c.669_670del	ENSP00000452896.1:p.Cys223TrpfsTer?
NM_000743.4:c.669_670del	NP_000734.2:p.Cys223TrpfsTer?
NM_001166694.1:c.669_670del	NP_001160166.1:p.Cys223TrpfsTer?
NR_046313.1:n.1170_1171del
XM_006720382.1:c.468_469del	XP_006720445.1:p.Cys156TrpfsTer?
XM_011521173.1:c.588_589del	XP_011519475.1:p.Cys196TrpfsTer?
XM_006720382.3:c.468_469del	XP_006720445.1:p.Cys156TrpfsTer?
NM_000743.5:c.669_670del MANE Select	NP_000734.2:p.Cys223TrpfsTer?
NM_001166694.2:c.669_670del	NP_001160166.1:p.Cys223TrpfsTer?
NR_046313.2:n.871_872del