Canonical Allele Identifier: CA2374743065

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350614T= , CM000682.2:g.63350614T=	GRCh38
NC_000020.10:g.61981966T= , CM000682.1:g.61981966T=	GRCh37
NC_000020.9:g.61452410T=	NCBI36
NG_011931.1:g.15730A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.797A= MANE Select	ENSP00000359285.4:p.Tyr266=
ENST00000370263.8:c.797A=	ENSP00000359285.4:p.Tyr266=
ENST00000463705.5:n.1445A=
ENST00000467563.3:n.867A=
ENST00000498043.6:c.821A=
ENST00000615287.4:c.584A=	ENSP00000483388.1:p.Tyr195=
ENST00000627000.1:c.*486A=	ENSP00000486914.1:n.*486A=
ENST00000630240.1:n.518A=
NM_000744.6:c.797A=	NP_000735.1:p.Tyr266=
NM_001256573.1:c.269A=	NP_001243502.1:p.Tyr90=
NR_046317.1:n.1053A=
XM_011528524.1:c.584A=	XP_011526826.1:p.Tyr195=
XM_017027625.2:c.269A=	XP_016883114.1:p.Tyr90=
XM_024451822.1:c.269A=	XP_024307590.1:p.Tyr90=
NM_001256573.2:c.269A=	NP_001243502.1:p.Tyr90=
NR_046317.2:n.1006A=
NM_000744.7:c.797A= MANE Select	NP_000735.1:p.Tyr266=