Canonical Allele Identifier: CA2189588831
Gene: CHRNA5 HGNC NCBI

Linked Data

dbSNP Id: rs2052963897

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78586635_78586641del , CM000677.2:g.78586635_78586641del GRCh38
NC_000015.9:g.78878977_78878983del , CM000677.1:g.78878977_78878983del GRCh37
NC_000015.8:g.76666032_76666038del NCBI36
NG_023328.1:g.26116_26122del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299565.9:c.259-10_259-4del MANE Select ENSP00000299565.5:n.259-10_259-4del
ENST00000394802.4:c.74-10_74-4del
ENST00000559554.5:c.259-10_259-4del ENSP00000453519.1:n.259-10_259-4del
NM_000745.3:c.259-10_259-4del NP_000736.2:n.259-10_259-4del
NM_001307945.1:c.259-10_259-4del NP_001294874.1:n.259-10_259-4del
XM_005254142.2:c.259-10_259-4del XP_005254199.1:n.259-10_259-4del
NM_001307945.2:c.259-10_259-4del NP_001294874.1:n.259-10_259-4del
NM_000745.4:c.259-10_259-4del MANE Select NP_000736.2:n.259-10_259-4del
NM_001395171.1:c.259-10_259-4del NP_001382100.1:n.259-10_259-4del
NM_001395172.1:c.259-10_259-4del NP_001382101.1:n.259-10_259-4del
NM_001395173.1:c.259-10_259-4del NP_001382102.1:n.259-10_259-4del
NM_001395174.1:c.259-10_259-4del NP_001382103.1:n.259-10_259-4del
NM_001395175.1:c.256-10_256-4del NP_001382104.1:n.256-10_256-4del