Canonical Allele Identifier: CA2374743206

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350863G= , CM000682.2:g.63350863G=	GRCh38
NC_000020.10:g.61982215G= , CM000682.1:g.61982215G=	GRCh37
NC_000020.9:g.61452659G=	NCBI36
NG_011931.1:g.15481C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.548C= MANE Select	ENSP00000359285.4:p.Thr183=
ENST00000370263.8:c.548C=	ENSP00000359285.4:p.Thr183=
ENST00000463705.5:n.1196C=
ENST00000467563.3:n.618C=
ENST00000498043.6:c.572C=
ENST00000615287.4:c.335C=	ENSP00000483388.1:p.Thr112=
ENST00000627000.1:c.*237C=	ENSP00000486914.1:n.*237C=
ENST00000630240.1:n.269C=
NM_000744.6:c.548C=	NP_000735.1:p.Thr183=
NM_001256573.1:c.20C=	NP_001243502.1:p.Thr7=
NR_046317.1:n.804C=
XM_011528524.1:c.335C=	XP_011526826.1:p.Thr112=
XM_017027625.2:c.20C=	XP_016883114.1:p.Thr7=
XM_024451822.1:c.20C=	XP_024307590.1:p.Thr7=
NM_001256573.2:c.20C=	NP_001243502.1:p.Thr7=
NR_046317.2:n.757C=
NM_000744.7:c.548C= MANE Select	NP_000735.1:p.Thr183=