Canonical Allele Identifier: CA273892781
Gene: CHRNA5 HGNC NCBI

Linked Data

dbSNP Id: rs998403338

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78586257_78586259del , CM000677.2:g.78586257_78586259del GRCh38
NC_000015.9:g.78878599_78878601del , CM000677.1:g.78878599_78878601del GRCh37
NC_000015.8:g.76665654_76665656del NCBI36
NG_023328.1:g.25738_25740del

Transcript Alleles

HGVS Amino-acid change
ENST00000299565.9:c.259-388_259-386del MANE Select ENSP00000299565.5:n.259-388_259-386del
ENST00000394802.4:c.74-388_74-386del
ENST00000559554.5:c.259-388_259-386del ENSP00000453519.1:n.259-388_259-386del
NM_000745.3:c.259-388_259-386del NP_000736.2:n.259-388_259-386del
NM_001307945.1:c.259-388_259-386del NP_001294874.1:n.259-388_259-386del
XM_005254142.2:c.259-388_259-386del XP_005254199.1:n.259-388_259-386del
NM_001307945.2:c.259-388_259-386del NP_001294874.1:n.259-388_259-386del
NM_000745.4:c.259-388_259-386del MANE Select NP_000736.2:n.259-388_259-386del
NM_001395171.1:c.259-388_259-386del NP_001382100.1:n.259-388_259-386del
NM_001395172.1:c.259-388_259-386del NP_001382101.1:n.259-388_259-386del
NM_001395173.1:c.259-388_259-386del NP_001382102.1:n.259-388_259-386del
NM_001395174.1:c.259-388_259-386del NP_001382103.1:n.259-388_259-386del
NM_001395175.1:c.256-388_256-386del NP_001382104.1:n.256-388_256-386del