Canonical Allele Identifier: CA2374742564
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63349763T= , CM000682.2:g.63349763T= GRCh38
NC_000020.10:g.61981115T= , CM000682.1:g.61981115T= GRCh37
NC_000020.9:g.61451559T= NCBI36
NG_011931.1:g.16581A=

Transcript Alleles

HGVS Amino-acid change
ENST00000370263.9:c.1648A= MANE Select ENSP00000359285.4:p.Ser550=
ENST00000370263.8:c.1648A= ENSP00000359285.4:p.Ser550=
ENST00000463705.5:n.2296A=
ENST00000467563.3:n.1718A=
ENST00000498043.6:c.1672A=
ENST00000615287.4:c.1435A= ENSP00000483388.1:p.Ser479=
ENST00000627000.1:c.*1337A= ENSP00000486914.1:n.*1337A=
ENST00000630240.1:n.1369A=
NM_000744.6:c.1648A= NP_000735.1:p.Ser550=
NM_001256573.1:c.1120A= NP_001243502.1:p.Ser374=
NR_046317.1:n.1904A=
XM_011528524.1:c.1435A= XP_011526826.1:p.Ser479=
XM_017027625.2:c.1120A= XP_016883114.1:p.Ser374=
XM_024451822.1:c.1120A= XP_024307590.1:p.Ser374=
NM_001256573.2:c.1120A= NP_001243502.1:p.Ser374=
NR_046317.2:n.1857A=
NM_000744.7:c.1648A= MANE Select NP_000735.1:p.Ser550=