Canonical Allele Identifier: CA1019264373
Gene: CHRNA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350744_63350751del , CM000682.2:g.63350744_63350751del GRCh38
NC_000020.10:g.61982096_61982103del , CM000682.1:g.61982096_61982103del GRCh37
NC_000020.9:g.61452540_61452547del NCBI36
NG_011931.1:g.15593_15600del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.660_667del MANE Select ENSP00000359285.4:p.Lys222ValfsTer?
ENST00000370263.8:c.660_667del ENSP00000359285.4:p.Lys222ValfsTer?
ENST00000463705.5:n.1308_1315del
ENST00000467563.3:n.730_737del
ENST00000498043.6:c.684_691del
ENST00000615287.4:c.447_454del ENSP00000483388.1:p.Lys151ValfsTer?
ENST00000627000.1:c.*349_*356del ENSP00000486914.1:n.*349_*356del
ENST00000630240.1:n.381_388del
NM_000744.6:c.660_667del NP_000735.1:p.Lys222ValfsTer?
NM_001256573.1:c.132_139del NP_001243502.1:p.Lys46ValfsTer?
NR_046317.1:n.916_923del
XM_011528524.1:c.447_454del XP_011526826.1:p.Lys151ValfsTer?
XM_017027625.2:c.132_139del XP_016883114.1:p.Lys46ValfsTer?
XM_024451822.1:c.132_139del XP_024307590.1:p.Lys46ValfsTer?
NM_001256573.2:c.132_139del NP_001243502.1:p.Lys46ValfsTer?
NR_046317.2:n.869_876del
NM_000744.7:c.660_667del MANE Select NP_000735.1:p.Lys222ValfsTer?