Canonical Allele Identifier: CA2374742936

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350382C= , CM000682.2:g.63350382C=	GRCh38
NC_000020.10:g.61981734C= , CM000682.1:g.61981734C=	GRCh37
NC_000020.9:g.61452178C=	NCBI36
NG_011931.1:g.15962G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1029G= MANE Select	ENSP00000359285.4:p.Trp343=
ENST00000370263.8:c.1029G=	ENSP00000359285.4:p.Trp343=
ENST00000463705.5:n.1677G=
ENST00000467563.3:n.1099G=
ENST00000498043.6:c.1053G=
ENST00000615287.4:c.816G=	ENSP00000483388.1:p.Trp272=
ENST00000627000.1:c.*718G=	ENSP00000486914.1:n.*718G=
ENST00000630240.1:n.750G=
NM_000744.6:c.1029G=	NP_000735.1:p.Trp343=
NM_001256573.1:c.501G=	NP_001243502.1:p.Trp167=
NR_046317.1:n.1285G=
XM_011528524.1:c.816G=	XP_011526826.1:p.Trp272=
XM_017027625.2:c.501G=	XP_016883114.1:p.Trp167=
XM_024451822.1:c.501G=	XP_024307590.1:p.Trp167=
NM_001256573.2:c.501G=	NP_001243502.1:p.Trp167=
NR_046317.2:n.1238G=
NM_000744.7:c.1029G= MANE Select	NP_000735.1:p.Trp343=