Canonical Allele Identifier: CA2374742961

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350426T= , CM000682.2:g.63350426T=	GRCh38
NC_000020.10:g.61981778T= , CM000682.1:g.61981778T=	GRCh37
NC_000020.9:g.61452222T=	NCBI36
NG_011931.1:g.15918A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.985A= MANE Select	ENSP00000359285.4:p.Asn329=
ENST00000370263.8:c.985A=	ENSP00000359285.4:p.Asn329=
ENST00000463705.5:n.1633A=
ENST00000467563.3:n.1055A=
ENST00000498043.6:c.1009A=
ENST00000615287.4:c.772A=	ENSP00000483388.1:p.Asn258=
ENST00000627000.1:c.*674A=	ENSP00000486914.1:n.*674A=
ENST00000630240.1:n.706A=
NM_000744.6:c.985A=	NP_000735.1:p.Asn329=
NM_001256573.1:c.457A=	NP_001243502.1:p.Asn153=
NR_046317.1:n.1241A=
XM_011528524.1:c.772A=	XP_011526826.1:p.Asn258=
XM_017027625.2:c.457A=	XP_016883114.1:p.Asn153=
XM_024451822.1:c.457A=	XP_024307590.1:p.Asn153=
NM_001256573.2:c.457A=	NP_001243502.1:p.Asn153=
NR_046317.2:n.1194A=
NM_000744.7:c.985A= MANE Select	NP_000735.1:p.Asn329=