Canonical Allele Identifier: CA715975109

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1206122302
• gnomAD v4: 15-78617155-G-GGA
• MyVariant Identifiers: chr15:g.78909497_78909498insGA (hg19) ; chr15:g.78617155_78617156insGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78617158_78617159dup , CM000677.2:g.78617158_78617159dup	GRCh38
NC_000015.9:g.78909500_78909501dup , CM000677.1:g.78909500_78909501dup	GRCh37
NC_000015.8:g.76696555_76696556dup	NCBI36
NG_016143.1:g.9139_9140dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000326828.6:c.268-24_268-23dup MANE Select	ENSP00000315602.5:n.268-24_268-23dup
ENST00000326828.5:c.268-24_268-23dup	ENSP00000315602.5:n.268-24_268-23dup
ENST00000348639.7:c.268-24_268-23dup	ENSP00000267951.4:n.268-24_268-23dup
ENST00000559658.5:c.268-24_268-23dup	ENSP00000452896.1:n.268-24_268-23dup
NM_000743.4:c.268-24_268-23dup	NP_000734.2:n.268-24_268-23dup
NM_001166694.1:c.268-24_268-23dup	NP_001160166.1:n.268-24_268-23dup
NR_046313.1:n.769-24_769-23dup
XM_006720382.1:c.67-24_67-23dup	XP_006720445.1:n.67-24_67-23dup
XM_011521173.1:c.187-24_187-23dup	XP_011519475.1:n.187-24_187-23dup
XM_006720382.3:c.67-24_67-23dup	XP_006720445.1:n.67-24_67-23dup
NM_000743.5:c.268-24_268-23dup MANE Select	NP_000734.2:n.268-24_268-23dup
NM_001166694.2:c.268-24_268-23dup	NP_001160166.1:n.268-24_268-23dup
NR_046313.2:n.470-24_470-23dup