Canonical Allele Identifier: CA2374743070
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350621C= , CM000682.2:g.63350621C= GRCh38
NC_000020.10:g.61981973C= , CM000682.1:g.61981973C= GRCh37
NC_000020.9:g.61452417C= NCBI36
NG_011931.1:g.15723G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.790G= MANE Select ENSP00000359285.4:p.Val264=
ENST00000370263.8:c.790G= ENSP00000359285.4:p.Val264=
ENST00000463705.5:n.1438G=
ENST00000467563.3:n.860G=
ENST00000498043.6:c.814G=
ENST00000615287.4:c.577G= ENSP00000483388.1:p.Val193=
ENST00000627000.1:c.*479G= ENSP00000486914.1:n.*479G=
ENST00000630240.1:n.511G=
NM_000744.6:c.790G= NP_000735.1:p.Val264=
NM_001256573.1:c.262G= NP_001243502.1:p.Val88=
NR_046317.1:n.1046G=
XM_011528524.1:c.577G= XP_011526826.1:p.Val193=
XM_017027625.2:c.262G= XP_016883114.1:p.Val88=
XM_024451822.1:c.262G= XP_024307590.1:p.Val88=
NM_001256573.2:c.262G= NP_001243502.1:p.Val88=
NR_046317.2:n.999G=
NM_000744.7:c.790G= MANE Select NP_000735.1:p.Val264=