Canonical Allele Identifier: CA2189588407
Gene: CHRNA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78586273A= , CM000677.2:g.78586273A= GRCh38
NC_000015.9:g.78878615A= , CM000677.1:g.78878615A= GRCh37
NC_000015.8:g.76665670A= NCBI36
NG_023328.1:g.25754A=

Transcript Alleles

HGVS Amino-acid change
ENST00000299565.9:c.259-372A= MANE Select ENSP00000299565.5:n.259-372A=
ENST00000394802.4:c.74-372A=
ENST00000559554.5:c.259-372A= ENSP00000453519.1:n.259-372A=
NM_000745.3:c.259-372A= NP_000736.2:n.259-372A=
NM_001307945.1:c.259-372A= NP_001294874.1:n.259-372A=
XM_005254142.2:c.259-372A= XP_005254199.1:n.259-372A=
NM_001307945.2:c.259-372A= NP_001294874.1:n.259-372A=
NM_000745.4:c.259-372A= MANE Select NP_000736.2:n.259-372A=
NM_001395171.1:c.259-372A= NP_001382100.1:n.259-372A=
NM_001395172.1:c.259-372A= NP_001382101.1:n.259-372A=
NM_001395173.1:c.259-372A= NP_001382102.1:n.259-372A=
NM_001395174.1:c.259-372A= NP_001382103.1:n.259-372A=
NM_001395175.1:c.256-372A= NP_001382104.1:n.256-372A=