Canonical Allele Identifier: CA2189589247
Gene: CHRNA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78586969G= , CM000677.2:g.78586969G= GRCh38
NC_000015.9:g.78879311G= , CM000677.1:g.78879311G= GRCh37
NC_000015.8:g.76666366G= NCBI36
NG_023328.1:g.26450G=

Transcript Alleles

HGVS Amino-acid change
ENST00000299565.9:c.303+280G= MANE Select ENSP00000299565.5:n.303+280G=
ENST00000394802.4:c.118+280G=
ENST00000559554.5:c.303+280G= ENSP00000453519.1:n.303+280G=
NM_000745.3:c.303+280G= NP_000736.2:n.303+280G=
NM_001307945.1:c.303+280G= NP_001294874.1:n.303+280G=
XM_005254142.2:c.303+280G= XP_005254199.1:n.303+280G=
NM_001307945.2:c.303+280G= NP_001294874.1:n.303+280G=
NM_000745.4:c.303+280G= MANE Select NP_000736.2:n.303+280G=
NM_001395171.1:c.303+280G= NP_001382100.1:n.303+280G=
NM_001395172.1:c.303+280G= NP_001382101.1:n.303+280G=
NM_001395173.1:c.303+280G= NP_001382102.1:n.303+280G=
NM_001395174.1:c.303+280G= NP_001382103.1:n.303+280G=
NM_001395175.1:c.300+280G= NP_001382104.1:n.300+280G=