Canonical Allele Identifier: CA2374742956

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350416T= , CM000682.2:g.63350416T=	GRCh38
NC_000020.10:g.61981768T= , CM000682.1:g.61981768T=	GRCh37
NC_000020.9:g.61452212T=	NCBI36
NG_011931.1:g.15928A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.995A= MANE Select	ENSP00000359285.4:p.His332=
ENST00000370263.8:c.995A=	ENSP00000359285.4:p.His332=
ENST00000463705.5:n.1643A=
ENST00000467563.3:n.1065A=
ENST00000498043.6:c.1019A=
ENST00000615287.4:c.782A=	ENSP00000483388.1:p.His261=
ENST00000627000.1:c.*684A=	ENSP00000486914.1:n.*684A=
ENST00000630240.1:n.716A=
NM_000744.6:c.995A=	NP_000735.1:p.His332=
NM_001256573.1:c.467A=	NP_001243502.1:p.His156=
NR_046317.1:n.1251A=
XM_011528524.1:c.782A=	XP_011526826.1:p.His261=
XM_017027625.2:c.467A=	XP_016883114.1:p.His156=
XM_024451822.1:c.467A=	XP_024307590.1:p.His156=
NM_001256573.2:c.467A=	NP_001243502.1:p.His156=
NR_046317.2:n.1204A=
NM_000744.7:c.995A= MANE Select	NP_000735.1:p.His332=