Canonical Allele Identifier: CA2374743105
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350687G= , CM000682.2:g.63350687G= GRCh38
NC_000020.10:g.61982039G= , CM000682.1:g.61982039G= GRCh37
NC_000020.9:g.61452483G= NCBI36
NG_011931.1:g.15657C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.724C= MANE Select ENSP00000359285.4:p.Leu242=
ENST00000370263.8:c.724C= ENSP00000359285.4:p.Leu242=
ENST00000463705.5:n.1372C=
ENST00000467563.3:n.794C=
ENST00000498043.6:c.748C=
ENST00000615287.4:c.511C= ENSP00000483388.1:p.Leu171=
ENST00000627000.1:c.*413C= ENSP00000486914.1:n.*413C=
ENST00000630240.1:n.445C=
NM_000744.6:c.724C= NP_000735.1:p.Leu242=
NM_001256573.1:c.196C= NP_001243502.1:p.Leu66=
NR_046317.1:n.980C=
XM_011528524.1:c.511C= XP_011526826.1:p.Leu171=
XM_017027625.2:c.196C= XP_016883114.1:p.Leu66=
XM_024451822.1:c.196C= XP_024307590.1:p.Leu66=
NM_001256573.2:c.196C= NP_001243502.1:p.Leu66=
NR_046317.2:n.933C=
NM_000744.7:c.724C= MANE Select NP_000735.1:p.Leu242=