Canonical Allele Identifier: CA2629788892
Gene: CHRNA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601821del , CM000677.2:g.78601821del GRCh38
NC_000015.9:g.78894163del , CM000677.1:g.78894163del GRCh37
NC_000015.8:g.76681218del NCBI36
NG_016143.1:g.24477del

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.823del MANE Select ENSP00000315602.5:p.Leu275CysfsTer9
ENST00000326828.5:c.823del ENSP00000315602.5:p.Leu275CysfsTer9
ENST00000348639.7:c.823del ENSP00000267951.4:p.Leu275CysfsTer9
ENST00000558903.1:n.530del
ENST00000559658.5:c.823del ENSP00000452896.1:p.Leu275CysfsTer9
NM_000743.4:c.823del NP_000734.2:p.Leu275CysfsTer9
NM_001166694.1:c.823del NP_001160166.1:p.Leu275CysfsTer9
NR_046313.1:n.1324del
XM_006720382.1:c.622del XP_006720445.1:p.Leu208CysfsTer9
XM_011521173.1:c.742del XP_011519475.1:p.Leu248CysfsTer9
XM_006720382.3:c.622del XP_006720445.1:p.Leu208CysfsTer9
NM_000743.5:c.823del MANE Select NP_000734.2:p.Leu275CysfsTer9
NM_001166694.2:c.823del NP_001160166.1:p.Leu275CysfsTer9
NR_046313.2:n.1025del