Canonical Allele Identifier: CA2374742972

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350448G= , CM000682.2:g.63350448G=	GRCh38
NC_000020.10:g.61981800G= , CM000682.1:g.61981800G=	GRCh37
NC_000020.9:g.61452244G=	NCBI36
NG_011931.1:g.15896C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.963C= MANE Select	ENSP00000359285.4:p.Ile321=
ENST00000370263.8:c.963C=	ENSP00000359285.4:p.Ile321=
ENST00000463705.5:n.1611C=
ENST00000467563.3:n.1033C=
ENST00000498043.6:c.987C=
ENST00000615287.4:c.750C=	ENSP00000483388.1:p.Ile250=
ENST00000627000.1:c.*652C=	ENSP00000486914.1:n.*652C=
ENST00000630240.1:n.684C=
NM_000744.6:c.963C=	NP_000735.1:p.Ile321=
NM_001256573.1:c.435C=	NP_001243502.1:p.Ile145=
NR_046317.1:n.1219C=
XM_011528524.1:c.750C=	XP_011526826.1:p.Ile250=
XM_017027625.2:c.435C=	XP_016883114.1:p.Ile145=
XM_024451822.1:c.435C=	XP_024307590.1:p.Ile145=
NM_001256573.2:c.435C=	NP_001243502.1:p.Ile145=
NR_046317.2:n.1172C=
NM_000744.7:c.963C= MANE Select	NP_000735.1:p.Ile321=