Canonical Allele Identifier: CA715974910
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs1357730525

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78617058_78617060del , CM000677.2:g.78617058_78617060del GRCh38
NC_000015.9:g.78909400_78909402del , CM000677.1:g.78909400_78909402del GRCh37
NC_000015.8:g.76696455_76696457del NCBI36
NG_016143.1:g.9239_9241del

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.344_346del MANE Select ENSP00000315602.5:p.Lys115del
ENST00000326828.5:c.344_346del ENSP00000315602.5:p.Lys115del
ENST00000348639.7:c.344_346del ENSP00000267951.4:p.Lys115del
ENST00000559658.5:c.344_346del ENSP00000452896.1:p.Lys115del
NM_000743.4:c.344_346del NP_000734.2:p.Lys115del
NM_001166694.1:c.344_346del NP_001160166.1:p.Lys115del
NR_046313.1:n.845_847del
XM_006720382.1:c.143_145del XP_006720445.1:p.Lys48del
XM_011521173.1:c.263_265del XP_011519475.1:p.Lys88del
XM_006720382.3:c.143_145del XP_006720445.1:p.Lys48del
NM_000743.5:c.344_346del MANE Select NP_000734.2:p.Lys115del
NM_001166694.2:c.344_346del NP_001160166.1:p.Lys115del
NR_046313.2:n.546_548del