Canonical Allele Identifier: CA2629788901
Gene: CHRNA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601875_78601877del , CM000677.2:g.78601875_78601877del GRCh38
NC_000015.9:g.78894217_78894219del , CM000677.1:g.78894217_78894219del GRCh37
NC_000015.8:g.76681272_76681274del NCBI36
NG_016143.1:g.24421_24423del

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.767_769del MANE Select ENSP00000315602.5:p.Ser256del
ENST00000326828.5:c.767_769del ENSP00000315602.5:p.Ser256del
ENST00000348639.7:c.767_769del ENSP00000267951.4:p.Ser256del
ENST00000558903.1:n.474_476del
ENST00000559658.5:c.767_769del ENSP00000452896.1:p.Ser256del
NM_000743.4:c.767_769del NP_000734.2:p.Ser256del
NM_001166694.1:c.767_769del NP_001160166.1:p.Ser256del
NR_046313.1:n.1268_1270del
XM_006720382.1:c.566_568del XP_006720445.1:p.Ser189del
XM_011521173.1:c.686_688del XP_011519475.1:p.Ser229del
XM_006720382.3:c.566_568del XP_006720445.1:p.Ser189del
NM_000743.5:c.767_769del MANE Select NP_000734.2:p.Ser256del
NM_001166694.2:c.767_769del NP_001160166.1:p.Ser256del
NR_046313.2:n.969_971del