Canonical Allele Identifier: CA715963890
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs1351393781

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601828del , CM000677.2:g.78601828del GRCh38
NC_000015.9:g.78894170del , CM000677.1:g.78894170del GRCh37
NC_000015.8:g.76681225del NCBI36
NG_016143.1:g.24469del

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.815del MANE Select ENSP00000315602.5:p.Lys272ArgfsTer2
ENST00000326828.5:c.815del ENSP00000315602.5:p.Lys272ArgfsTer2
ENST00000348639.7:c.815del ENSP00000267951.4:p.Lys272ArgfsTer2
ENST00000558903.1:n.522del
ENST00000559658.5:c.815del ENSP00000452896.1:p.Lys272ArgfsTer2
NM_000743.4:c.815del NP_000734.2:p.Lys272ArgfsTer2
NM_001166694.1:c.815del NP_001160166.1:p.Lys272ArgfsTer2
NR_046313.1:n.1316del
XM_006720382.1:c.614del XP_006720445.1:p.Lys205ArgfsTer2
XM_011521173.1:c.734del XP_011519475.1:p.Lys245ArgfsTer2
XM_006720382.3:c.614del XP_006720445.1:p.Lys205ArgfsTer2
NM_000743.5:c.815del MANE Select NP_000734.2:p.Lys272ArgfsTer2
NM_001166694.2:c.815del NP_001160166.1:p.Lys272ArgfsTer2
NR_046313.2:n.1017del