Canonical Allele Identifier: CA2374743038

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350560G= , CM000682.2:g.63350560G=	GRCh38
NC_000020.10:g.61981912G= , CM000682.1:g.61981912G=	GRCh37
NC_000020.9:g.61452356G=	NCBI36
NG_011931.1:g.15784C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000744.7:c.851C= MANE Select	NP_000735.1:p.Ser284=
ENST00000370263.9:c.851C= MANE Select	ENSP00000359285.4:p.Ser284=
NM_000744.6:c.851C=	NP_000735.1:p.Ser284=
NM_001256573.1:c.323C=	NP_001243502.1:p.Ser108=
NM_001256573.2:c.323C=	NP_001243502.1:p.Ser108=
NR_046317.1:n.1107C=
NR_046317.2:n.1060C=
ENST00000370263.8:c.851C=	ENSP00000359285.4:p.Ser284=
ENST00000463705.5:n.1499C=
ENST00000467563.3:n.921C=
ENST00000498043.6:c.875C=
ENST00000615287.4:c.638C=	ENSP00000483388.1:p.Ser213=
ENST00000627000.1:c.*540C=	ENSP00000486914.1:n.*540C=
ENST00000630240.1:n.572C=
XM_011528524.1:c.638C=	XP_011526826.1:p.Ser213=
XM_017027625.2:c.323C=	XP_016883114.1:p.Ser108=
XM_024451822.1:c.323C=	XP_024307590.1:p.Ser108=