Canonical Allele Identifier: CA2374743231

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350918C= , CM000682.2:g.63350918C=	GRCh38
NC_000020.10:g.61982270C= , CM000682.1:g.61982270C=	GRCh37
NC_000020.9:g.61452714C=	NCBI36
NG_011931.1:g.15426G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.493G= MANE Select	ENSP00000359285.4:p.Val165=
ENST00000370263.8:c.493G=	ENSP00000359285.4:p.Val165=
ENST00000463705.5:n.1141G=
ENST00000467563.3:n.563G=
ENST00000498043.6:c.517G=
ENST00000615287.4:c.280G=	ENSP00000483388.1:p.Val94=
ENST00000627000.1:c.*182G=	ENSP00000486914.1:n.*182G=
ENST00000628665.1:n.536G=
ENST00000630240.1:n.214G=
NM_000744.6:c.493G=	NP_000735.1:p.Val165=
NM_001256573.1:c.-36G=	NP_001243502.1:n.-36G=
NR_046317.1:n.749G=
XM_011528524.1:c.280G=	XP_011526826.1:p.Val94=
XM_017027625.2:c.-36G=	XP_016883114.1:n.-36G=
XM_024451822.1:c.-36G=	XP_024307590.1:n.-36G=
NM_001256573.2:c.-36G=	NP_001243502.1:n.-36G=
NR_046317.2:n.702G=
NM_000744.7:c.493G= MANE Select	NP_000735.1:p.Val165=