Canonical Allele Identifier: CA7684552
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs778024498

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78617159_78617161del , CM000677.2:g.78617159_78617161del GRCh38
NC_000015.9:g.78909501_78909503del , CM000677.1:g.78909501_78909503del GRCh37
NC_000015.8:g.76696556_76696558del NCBI36
NG_016143.1:g.9137_9139del

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.268-26_268-24del MANE Select ENSP00000315602.5:n.268-26_268-24del
ENST00000326828.5:c.268-26_268-24del ENSP00000315602.5:n.268-26_268-24del
ENST00000348639.7:c.268-26_268-24del ENSP00000267951.4:n.268-26_268-24del
ENST00000559658.5:c.268-26_268-24del ENSP00000452896.1:n.268-26_268-24del
NM_000743.4:c.268-26_268-24del NP_000734.2:n.268-26_268-24del
NM_001166694.1:c.268-26_268-24del NP_001160166.1:n.268-26_268-24del
NR_046313.1:n.769-26_769-24del
XM_006720382.1:c.67-26_67-24del XP_006720445.1:n.67-26_67-24del
XM_011521173.1:c.187-26_187-24del XP_011519475.1:n.187-26_187-24del
XM_006720382.3:c.67-26_67-24del XP_006720445.1:n.67-26_67-24del
NM_000743.5:c.268-26_268-24del MANE Select NP_000734.2:n.268-26_268-24del
NM_001166694.2:c.268-26_268-24del NP_001160166.1:n.268-26_268-24del
NR_046313.2:n.470-26_470-24del