Canonical Allele Identifier: CA2374743042

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350570C= , CM000682.2:g.63350570C=	GRCh38
NC_000020.10:g.61981922C= , CM000682.1:g.61981922C=	GRCh37
NC_000020.9:g.61452366C=	NCBI36
NG_011931.1:g.15774G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.841G= MANE Select	ENSP00000359285.4:p.Val281=
ENST00000370263.8:c.841G=	ENSP00000359285.4:p.Val281=
ENST00000463705.5:n.1489G=
ENST00000467563.3:n.911G=
ENST00000498043.6:c.865G=
ENST00000615287.4:c.628G=	ENSP00000483388.1:p.Val210=
ENST00000627000.1:c.*530G=	ENSP00000486914.1:n.*530G=
ENST00000630240.1:n.562G=
NM_000744.6:c.841G=	NP_000735.1:p.Val281=
NM_001256573.1:c.313G=	NP_001243502.1:p.Val105=
NR_046317.1:n.1097G=
XM_011528524.1:c.628G=	XP_011526826.1:p.Val210=
XM_017027625.2:c.313G=	XP_016883114.1:p.Val105=
XM_024451822.1:c.313G=	XP_024307590.1:p.Val105=
NM_001256573.2:c.313G=	NP_001243502.1:p.Val105=
NR_046317.2:n.1050G=
NM_000744.7:c.841G= MANE Select	NP_000735.1:p.Val281=