Canonical Allele Identifier: CA715964915

Gene: CHRNA3

Linked Data

• dbSNP Id: rs1396955361
• gnomAD v3: 15-78602345-CAGTA-C
• gnomAD v4: 15-78602345-CAGTA-C
• MyVariant Identifiers: chr15:g.78894688_78894691del (hg19) ; chr15:g.78602346_78602349del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602351_78602354del , CM000677.2:g.78602351_78602354del	GRCh38
NC_000015.9:g.78894693_78894696del , CM000677.1:g.78894693_78894696del	GRCh37
NC_000015.8:g.76681748_76681751del	NCBI36
NG_016143.1:g.23947_23950del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.378-85_378-82del MANE Select	ENSP00000315602.5:n.378-85_378-82del
ENST00000326828.5:c.378-85_378-82del	ENSP00000315602.5:n.378-85_378-82del
ENST00000348639.7:c.378-85_378-82del	ENSP00000267951.4:n.378-85_378-82del
ENST00000558903.1:n.85-85_85-82del
ENST00000559658.5:c.378-85_378-82del	ENSP00000452896.1:n.378-85_378-82del
NM_000743.4:c.378-85_378-82del	NP_000734.2:n.378-85_378-82del
NM_001166694.1:c.378-85_378-82del	NP_001160166.1:n.378-85_378-82del
NR_046313.1:n.879-85_879-82del
XM_006720382.1:c.177-85_177-82del	XP_006720445.1:n.177-85_177-82del
XM_011521173.1:c.297-85_297-82del	XP_011519475.1:n.297-85_297-82del
XM_006720382.3:c.177-85_177-82del	XP_006720445.1:n.177-85_177-82del
NM_000743.5:c.378-85_378-82del MANE Select	NP_000734.2:n.378-85_378-82del
NM_001166694.2:c.378-85_378-82del	NP_001160166.1:n.378-85_378-82del
NR_046313.2:n.580-85_580-82del