Canonical Allele Identifier: CA2374742989

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350472G= , CM000682.2:g.63350472G=	GRCh38
NC_000020.10:g.61981824G= , CM000682.1:g.61981824G=	GRCh37
NC_000020.9:g.61452268G=	NCBI36
NG_011931.1:g.15872C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.939C= MANE Select	ENSP00000359285.4:p.Thr313=
ENST00000370263.8:c.939C=	ENSP00000359285.4:p.Thr313=
ENST00000463705.5:n.1587C=
ENST00000467563.3:n.1009C=
ENST00000498043.6:c.963C=
ENST00000615287.4:c.726C=	ENSP00000483388.1:p.Thr242=
ENST00000627000.1:c.*628C=	ENSP00000486914.1:n.*628C=
ENST00000630240.1:n.660C=
NM_000744.6:c.939C=	NP_000735.1:p.Thr313=
NM_001256573.1:c.411C=	NP_001243502.1:p.Thr137=
NR_046317.1:n.1195C=
XM_011528524.1:c.726C=	XP_011526826.1:p.Thr242=
XM_017027625.2:c.411C=	XP_016883114.1:p.Thr137=
XM_024451822.1:c.411C=	XP_024307590.1:p.Thr137=
NM_001256573.2:c.411C=	NP_001243502.1:p.Thr137=
NR_046317.2:n.1148C=
NM_000744.7:c.939C= MANE Select	NP_000735.1:p.Thr313=