Canonical Allele Identifier: CA2538108347
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78599276_78599295del , CM000677.2:g.78599276_78599295del GRCh38
NC_000015.9:g.78891618_78891637del , CM000677.1:g.78891618_78891637del GRCh37
NC_000015.8:g.76678673_76678692del NCBI36
NG_016143.1:g.27001_27020del

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.1389+1958_1389+1977del MANE Select ENSP00000315602.5:n.1389+1958_1389+1977de...
ENST00000326828.5:c.1389+1958_1389+1977del ENSP00000315602.5:n.1389+1958_1389+1977de...
ENST00000348639.7:c.1389+1958_1389+1977del ENSP00000267951.4:n.1389+1958_1389+1977de...
ENST00000559658.5:c.1389+1958_1389+1977del ENSP00000452896.1:n.1389+1958_1389+1977de...
NM_000743.4:c.1389+1958_1389+1977del NP_000734.2:n.1389+1958_1389+1977del
NM_001166694.1:c.1389+1958_1389+1977del NP_001160166.1:n.1389+1958_1389+1977del
NR_046313.1:n.1890+1958_1890+1977del
XM_006720382.1:c.1188+1958_1188+1977del XP_006720445.1:n.1188+1958_1188+1977del
XM_011521173.1:c.1308+1958_1308+1977del XP_011519475.1:n.1308+1958_1308+1977del
XM_006720382.3:c.1188+1958_1188+1977del XP_006720445.1:n.1188+1958_1188+1977del
NM_000743.5:c.1389+1958_1389+1977del MANE Select NP_000734.2:n.1389+1958_1389+1977del
NM_001166694.2:c.1389+1958_1389+1977del NP_001160166.1:n.1389+1958_1389+1977del
NR_046313.2:n.1591+1958_1591+1977del