Canonical Allele Identifier: CA2374742918

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350351G= , CM000682.2:g.63350351G=	GRCh38
NC_000020.10:g.61981703G= , CM000682.1:g.61981703G=	GRCh37
NC_000020.9:g.61452147G=	NCBI36
NG_011931.1:g.15993C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1060C= MANE Select	ENSP00000359285.4:p.Arg354=
ENST00000370263.8:c.1060C=	ENSP00000359285.4:p.Arg354=
ENST00000463705.5:n.1708C=
ENST00000467563.3:n.1130C=
ENST00000498043.6:c.1084C=
ENST00000615287.4:c.847C=	ENSP00000483388.1:p.Arg283=
ENST00000627000.1:c.*749C=	ENSP00000486914.1:n.*749C=
ENST00000630240.1:n.781C=
NM_000744.6:c.1060C=	NP_000735.1:p.Arg354=
NM_001256573.1:c.532C=	NP_001243502.1:p.Arg178=
NR_046317.1:n.1316C=
XM_011528524.1:c.847C=	XP_011526826.1:p.Arg283=
XM_017027625.2:c.532C=	XP_016883114.1:p.Arg178=
XM_024451822.1:c.532C=	XP_024307590.1:p.Arg178=
NM_001256573.2:c.532C=	NP_001243502.1:p.Arg178=
NR_046317.2:n.1269C=
NM_000744.7:c.1060C= MANE Select	NP_000735.1:p.Arg354=