Canonical Allele Identifier: CA2653784394
Gene: CHRNA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350733_63350734insGG , CM000682.2:g.63350733_63350734insGG GRCh38
NC_000020.10:g.61982085_61982086insGG , CM000682.1:g.61982085_61982086insGG GRCh37
NC_000020.9:g.61452529_61452530insGG NCBI36
NG_011931.1:g.15610_15611insCC

Transcript Alleles

HGVS Amino-acid change
ENST00000370263.9:c.677_678insCC MANE Select ENSP00000359285.4:p.Ala227LeufsTer?
ENST00000370263.8:c.677_678insCC ENSP00000359285.4:p.Ala227LeufsTer?
ENST00000463705.5:n.1325_1326insCC
ENST00000467563.3:n.747_748insCC
ENST00000498043.6:c.701_702insCC
ENST00000615287.4:c.464_465insCC ENSP00000483388.1:p.Ala156LeufsTer?
ENST00000627000.1:c.*366_*367insCC ENSP00000486914.1:n.*366_*367insCC
ENST00000630240.1:n.398_399insCC
NM_000744.6:c.677_678insCC NP_000735.1:p.Ala227LeufsTer?
NM_001256573.1:c.149_150insCC NP_001243502.1:p.Ala51LeufsTer?
NR_046317.1:n.933_934insCC
XM_011528524.1:c.464_465insCC XP_011526826.1:p.Ala156LeufsTer?
XM_017027625.2:c.149_150insCC XP_016883114.1:p.Ala51LeufsTer?
XM_024451822.1:c.149_150insCC XP_024307590.1:p.Ala51LeufsTer?
NM_001256573.2:c.149_150insCC NP_001243502.1:p.Ala51LeufsTer?
NR_046317.2:n.886_887insCC
NM_000744.7:c.677_678insCC MANE Select NP_000735.1:p.Ala227LeufsTer?