Canonical Allele Identifier: CA2374742973

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350449A= , CM000682.2:g.63350449A=	GRCh38
NC_000020.10:g.61981801A= , CM000682.1:g.61981801A=	GRCh37
NC_000020.9:g.61452245A=	NCBI36
NG_011931.1:g.15895T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.962T= MANE Select	ENSP00000359285.4:p.Ile321=
ENST00000370263.8:c.962T=	ENSP00000359285.4:p.Ile321=
ENST00000463705.5:n.1610T=
ENST00000467563.3:n.1032T=
ENST00000498043.6:c.986T=
ENST00000615287.4:c.749T=	ENSP00000483388.1:p.Ile250=
ENST00000627000.1:c.*651T=	ENSP00000486914.1:n.*651T=
ENST00000630240.1:n.683T=
NM_000744.6:c.962T=	NP_000735.1:p.Ile321=
NM_001256573.1:c.434T=	NP_001243502.1:p.Ile145=
NR_046317.1:n.1218T=
XM_011528524.1:c.749T=	XP_011526826.1:p.Ile250=
XM_017027625.2:c.434T=	XP_016883114.1:p.Ile145=
XM_024451822.1:c.434T=	XP_024307590.1:p.Ile145=
NM_001256573.2:c.434T=	NP_001243502.1:p.Ile145=
NR_046317.2:n.1171T=
NM_000744.7:c.962T= MANE Select	NP_000735.1:p.Ile321=