Canonical Allele Identifier: CA715964929

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1256040151
• MyVariant Identifiers: chr15:g.78894711_78894712insTGGAAGATGA (hg19) ; chr15:g.78602369_78602370insTGGAAGATGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602370_78602379dup , CM000677.2:g.78602370_78602379dup	GRCh38
NC_000015.9:g.78894712_78894721dup , CM000677.1:g.78894712_78894721dup	GRCh37
NC_000015.8:g.76681767_76681776dup	NCBI36
NG_016143.1:g.23917_23926dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.378-115_378-106dup MANE Select	ENSP00000315602.5:n.378-115_378-106dup
ENST00000326828.5:c.378-115_378-106dup	ENSP00000315602.5:n.378-115_378-106dup
ENST00000348639.7:c.378-115_378-106dup	ENSP00000267951.4:n.378-115_378-106dup
ENST00000558903.1:n.85-115_85-106dup
ENST00000559658.5:c.378-115_378-106dup	ENSP00000452896.1:n.378-115_378-106dup
NM_000743.4:c.378-115_378-106dup	NP_000734.2:n.378-115_378-106dup
NM_001166694.1:c.378-115_378-106dup	NP_001160166.1:n.378-115_378-106dup
NR_046313.1:n.879-115_879-106dup
XM_006720382.1:c.177-115_177-106dup	XP_006720445.1:n.177-115_177-106dup
XM_011521173.1:c.297-115_297-106dup	XP_011519475.1:n.297-115_297-106dup
XM_006720382.3:c.177-115_177-106dup	XP_006720445.1:n.177-115_177-106dup
NM_000743.5:c.378-115_378-106dup MANE Select	NP_000734.2:n.378-115_378-106dup
NM_001166694.2:c.378-115_378-106dup	NP_001160166.1:n.378-115_378-106dup
NR_046313.2:n.580-115_580-106dup