Canonical Allele Identifier: CA2189591957
Gene: CHRNA5 HGNC NCBI

Linked Data

dbSNP Id: rs2052989871

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78589444_78589455del , CM000677.2:g.78589444_78589455del GRCh38
NC_000015.9:g.78881786_78881797del , CM000677.1:g.78881786_78881797del GRCh37
NC_000015.8:g.76668841_76668852del NCBI36
NG_023328.1:g.28925_28936del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299565.9:c.414-361_414-350del MANE Select ENSP00000299565.5:n.414-361_414-350del
ENST00000394802.4:c.229-361_229-350del
ENST00000559554.5:c.414-361_414-350del ENSP00000453519.1:n.414-361_414-350del
NM_000745.3:c.414-361_414-350del NP_000736.2:n.414-361_414-350del
NM_001307945.1:c.414-361_414-350del NP_001294874.1:n.414-361_414-350del
XM_005254142.2:c.414-361_414-350del XP_005254199.1:n.414-361_414-350del
NM_001307945.2:c.414-361_414-350del NP_001294874.1:n.414-361_414-350del
NM_000745.4:c.414-361_414-350del MANE Select NP_000736.2:n.414-361_414-350del
NM_001395171.1:c.414-361_414-350del NP_001382100.1:n.414-361_414-350del
NM_001395172.1:c.414-361_414-350del NP_001382101.1:n.414-361_414-350del
NM_001395173.1:c.414-361_414-350del NP_001382102.1:n.414-361_414-350del
NM_001395174.1:c.414-361_414-350del NP_001382103.1:n.414-361_414-350del
NM_001395175.1:c.411-361_411-350del NP_001382104.1:n.411-361_411-350del