Canonical Allele Identifier: CA1019264300
Gene: CHRNA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350735_63350741del , CM000682.2:g.63350735_63350741del GRCh38
NC_000020.10:g.61982087_61982093del , CM000682.1:g.61982087_61982093del GRCh37
NC_000020.9:g.61452531_61452537del NCBI36
NG_011931.1:g.15604_15610del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.671_677del MANE Select ENSP00000359285.4:p.Glu224ValfsTer?
ENST00000370263.8:c.671_677del ENSP00000359285.4:p.Glu224ValfsTer?
ENST00000463705.5:n.1319_1325del
ENST00000467563.3:n.741_747del
ENST00000498043.6:c.695_701del
ENST00000615287.4:c.458_464del ENSP00000483388.1:p.Glu153ValfsTer?
ENST00000627000.1:c.*360_*366del ENSP00000486914.1:n.*360_*366del
ENST00000630240.1:n.392_398del
NM_000744.6:c.671_677del NP_000735.1:p.Glu224ValfsTer?
NM_001256573.1:c.143_149del NP_001243502.1:p.Glu48ValfsTer?
NR_046317.1:n.927_933del
XM_011528524.1:c.458_464del XP_011526826.1:p.Glu153ValfsTer?
XM_017027625.2:c.143_149del XP_016883114.1:p.Glu48ValfsTer?
XM_024451822.1:c.143_149del XP_024307590.1:p.Glu48ValfsTer?
NM_001256573.2:c.143_149del NP_001243502.1:p.Glu48ValfsTer?
NR_046317.2:n.880_886del
NM_000744.7:c.671_677del MANE Select NP_000735.1:p.Glu224ValfsTer?