Canonical Allele Identifier: CA971783028
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs2053221754

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78602496_78602508del , CM000677.2:g.78602496_78602508del GRCh38
NC_000015.9:g.78894838_78894850del , CM000677.1:g.78894838_78894850del GRCh37
NC_000015.8:g.76681893_76681905del NCBI36
NG_016143.1:g.23792_23804del

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.378-240_378-228del MANE Select ENSP00000315602.5:n.378-240_378-228del
ENST00000326828.5:c.378-240_378-228del ENSP00000315602.5:n.378-240_378-228del
ENST00000348639.7:c.378-240_378-228del ENSP00000267951.4:n.378-240_378-228del
ENST00000558903.1:n.85-240_85-228del
ENST00000559658.5:c.378-240_378-228del ENSP00000452896.1:n.378-240_378-228del
NM_000743.4:c.378-240_378-228del NP_000734.2:n.378-240_378-228del
NM_001166694.1:c.378-240_378-228del NP_001160166.1:n.378-240_378-228del
NR_046313.1:n.879-240_879-228del
XM_006720382.1:c.177-240_177-228del XP_006720445.1:n.177-240_177-228del
XM_011521173.1:c.297-240_297-228del XP_011519475.1:n.297-240_297-228del
XM_006720382.3:c.177-240_177-228del XP_006720445.1:n.177-240_177-228del
NM_000743.5:c.378-240_378-228del MANE Select NP_000734.2:n.378-240_378-228del
NM_001166694.2:c.378-240_378-228del NP_001160166.1:n.378-240_378-228del
NR_046313.2:n.580-240_580-228del