Canonical Allele Identifier: CA2374742996

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350489C= , CM000682.2:g.63350489C=	GRCh38
NC_000020.10:g.61981841C= , CM000682.1:g.61981841C=	GRCh37
NC_000020.9:g.61452285C=	NCBI36
NG_011931.1:g.15855G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.922G= MANE Select	ENSP00000359285.4:p.Glu308=
ENST00000370263.8:c.922G=	ENSP00000359285.4:p.Glu308=
ENST00000463705.5:n.1570G=
ENST00000467563.3:n.992G=
ENST00000498043.6:c.946G=
ENST00000615287.4:c.709G=	ENSP00000483388.1:p.Glu237=
ENST00000627000.1:c.*611G=	ENSP00000486914.1:n.*611G=
ENST00000630240.1:n.643G=
NM_000744.6:c.922G=	NP_000735.1:p.Glu308=
NM_001256573.1:c.394G=	NP_001243502.1:p.Glu132=
NR_046317.1:n.1178G=
XM_011528524.1:c.709G=	XP_011526826.1:p.Glu237=
XM_017027625.2:c.394G=	XP_016883114.1:p.Glu132=
XM_024451822.1:c.394G=	XP_024307590.1:p.Glu132=
NM_001256573.2:c.394G=	NP_001243502.1:p.Glu132=
NR_046317.2:n.1131G=
NM_000744.7:c.922G= MANE Select	NP_000735.1:p.Glu308=