Canonical Allele Identifier: CA2374743054

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350595G= , CM000682.2:g.63350595G=	GRCh38
NC_000020.10:g.61981947G= , CM000682.1:g.61981947G=	GRCh37
NC_000020.9:g.61452391G=	NCBI36
NG_011931.1:g.15749C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.816C= MANE Select	ENSP00000359285.4:p.Gly272=
ENST00000370263.8:c.816C=	ENSP00000359285.4:p.Gly272=
ENST00000463705.5:n.1464C=
ENST00000467563.3:n.886C=
ENST00000498043.6:c.840C=
ENST00000615287.4:c.603C=	ENSP00000483388.1:p.Gly201=
ENST00000627000.1:c.*505C=	ENSP00000486914.1:n.*505C=
ENST00000630240.1:n.537C=
NM_000744.6:c.816C=	NP_000735.1:p.Gly272=
NM_001256573.1:c.288C=	NP_001243502.1:p.Gly96=
NR_046317.1:n.1072C=
XM_011528524.1:c.603C=	XP_011526826.1:p.Gly201=
XM_017027625.2:c.288C=	XP_016883114.1:p.Gly96=
XM_024451822.1:c.288C=	XP_024307590.1:p.Gly96=
NM_001256573.2:c.288C=	NP_001243502.1:p.Gly96=
NR_046317.2:n.1025C=
NM_000744.7:c.816C= MANE Select	NP_000735.1:p.Gly272=