Canonical Allele Identifier: CA2804872470
Gene: CHRNA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78586229_78586230insAAAA , CM000677.2:g.78586229_78586230insAAAA GRCh38
NC_000015.9:g.78878571_78878572insAAAA , CM000677.1:g.78878571_78878572insAAAA GRCh37
NC_000015.8:g.76665626_76665627insAAAA NCBI36
NG_023328.1:g.25710_25711insAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000299565.9:c.259-416_259-415insAAAA MANE Select ENSP00000299565.5:n.259-416_259-415insAAAA
ENST00000394802.4:c.74-416_74-415insAAAA
ENST00000559554.5:c.259-416_259-415insAAAA ENSP00000453519.1:n.259-416_259-415insAAAA
NM_000745.3:c.259-416_259-415insAAAA NP_000736.2:n.259-416_259-415insAAAA
NM_001307945.1:c.259-416_259-415insAAAA NP_001294874.1:n.259-416_259-415insAAAA
XM_005254142.2:c.259-416_259-415insAAAA XP_005254199.1:n.259-416_259-415insAAAA
NM_001307945.2:c.259-416_259-415insAAAA NP_001294874.1:n.259-416_259-415insAAAA
NM_000745.4:c.259-416_259-415insAAAA MANE Select NP_000736.2:n.259-416_259-415insAAAA
NM_001395171.1:c.259-416_259-415insAAAA NP_001382100.1:n.259-416_259-415insAAAA
NM_001395172.1:c.259-416_259-415insAAAA NP_001382101.1:n.259-416_259-415insAAAA
NM_001395173.1:c.259-416_259-415insAAAA NP_001382102.1:n.259-416_259-415insAAAA
NM_001395174.1:c.259-416_259-415insAAAA NP_001382103.1:n.259-416_259-415insAAAA
NM_001395175.1:c.256-416_256-415insAAAA NP_001382104.1:n.256-416_256-415insAAAA