Canonical Allele Identifier: CA2374743135
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350733A= , CM000682.2:g.63350733A= GRCh38
NC_000020.10:g.61982085A= , CM000682.1:g.61982085A= GRCh37
NC_000020.9:g.61452529A= NCBI36
NG_011931.1:g.15611T=

Transcript Alleles

HGVS Amino-acid Change
NM_000744.7:c.678T= MANE Select NP_000735.1:p.Cys226=
ENST00000370263.9:c.678T= MANE Select ENSP00000359285.4:p.Cys226=
NM_000744.6:c.678T= NP_000735.1:p.Cys226=
NM_001256573.1:c.150T= NP_001243502.1:p.Cys50=
NM_001256573.2:c.150T= NP_001243502.1:p.Cys50=
NR_046317.1:n.934T=
NR_046317.2:n.887T=
ENST00000370263.8:c.678T= ENSP00000359285.4:p.Cys226=
ENST00000463705.5:n.1326T=
ENST00000467563.3:n.748T=
ENST00000498043.6:c.702T=
ENST00000615287.4:c.465T= ENSP00000483388.1:p.Cys155=
ENST00000627000.1:c.*367T= ENSP00000486914.1:n.*367T=
ENST00000630240.1:n.399T=
XM_011528524.1:c.465T= XP_011526826.1:p.Cys155=
XM_017027625.2:c.150T= XP_016883114.1:p.Cys50=
XM_024451822.1:c.150T= XP_024307590.1:p.Cys50=