Canonical Allele Identifier: CA619417595
Gene: CHRNA3 HGNC NCBI

Linked Data

dbSNP Id: rs1444202915

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78602041_78602044dup , CM000677.2:g.78602041_78602044dup GRCh38
NC_000015.9:g.78894383_78894386dup , CM000677.1:g.78894383_78894386dup GRCh37
NC_000015.8:g.76681438_76681441dup NCBI36
NG_016143.1:g.24252_24255dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.598_601dup MANE Select ENSP00000315602.5:p.Tyr201Ter
ENST00000326828.5:c.598_601dup ENSP00000315602.5:p.Tyr201Ter
ENST00000348639.7:c.598_601dup ENSP00000267951.4:p.Tyr201Ter
ENST00000558903.1:n.305_308dup
ENST00000559658.5:c.598_601dup ENSP00000452896.1:p.Tyr201Ter
NM_000743.4:c.598_601dup NP_000734.2:p.Tyr201Ter
NM_001166694.1:c.598_601dup NP_001160166.1:p.Tyr201Ter
NR_046313.1:n.1099_1102dup
XM_006720382.1:c.397_400dup XP_006720445.1:p.Tyr134Ter
XM_011521173.1:c.517_520dup XP_011519475.1:p.Tyr174Ter
XM_006720382.3:c.397_400dup XP_006720445.1:p.Tyr134Ter
NM_000743.5:c.598_601dup MANE Select NP_000734.2:p.Tyr201Ter
NM_001166694.2:c.598_601dup NP_001160166.1:p.Tyr201Ter
NR_046313.2:n.800_803dup