Canonical Allele Identifier: CA2804873233
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78602333dup , CM000677.2:g.78602333dup GRCh38
NC_000015.9:g.78894675dup , CM000677.1:g.78894675dup GRCh37
NC_000015.8:g.76681730dup NCBI36
NG_016143.1:g.23964dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.378-68dup MANE Select ENSP00000315602.5:n.378-68dup
ENST00000326828.5:c.378-68dup ENSP00000315602.5:n.378-68dup
ENST00000348639.7:c.378-68dup ENSP00000267951.4:n.378-68dup
ENST00000558903.1:n.85-68dup
ENST00000559658.5:c.378-68dup ENSP00000452896.1:n.378-68dup
NM_000743.4:c.378-68dup NP_000734.2:n.378-68dup
NM_001166694.1:c.378-68dup NP_001160166.1:n.378-68dup
NR_046313.1:n.879-68dup
XM_006720382.1:c.177-68dup XP_006720445.1:n.177-68dup
XM_011521173.1:c.297-68dup XP_011519475.1:n.297-68dup
XM_006720382.3:c.177-68dup XP_006720445.1:n.177-68dup
NM_000743.5:c.378-68dup MANE Select NP_000734.2:n.378-68dup
NM_001166694.2:c.378-68dup NP_001160166.1:n.378-68dup
NR_046313.2:n.580-68dup