Canonical Allele Identifier: CA2374742910

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350336T= , CM000682.2:g.63350336T=	GRCh38
NC_000020.10:g.61981688T= , CM000682.1:g.61981688T=	GRCh37
NC_000020.9:g.61452132T=	NCBI36
NG_011931.1:g.16008A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1075A= MANE Select	ENSP00000359285.4:p.Lys359=
ENST00000370263.8:c.1075A=	ENSP00000359285.4:p.Lys359=
ENST00000463705.5:n.1723A=
ENST00000467563.3:n.1145A=
ENST00000498043.6:c.1099A=
ENST00000615287.4:c.862A=	ENSP00000483388.1:p.Lys288=
ENST00000627000.1:c.*764A=	ENSP00000486914.1:n.*764A=
ENST00000630240.1:n.796A=
NM_000744.6:c.1075A=	NP_000735.1:p.Lys359=
NM_001256573.1:c.547A=	NP_001243502.1:p.Lys183=
NR_046317.1:n.1331A=
XM_011528524.1:c.862A=	XP_011526826.1:p.Lys288=
XM_017027625.2:c.547A=	XP_016883114.1:p.Lys183=
XM_024451822.1:c.547A=	XP_024307590.1:p.Lys183=
NM_001256573.2:c.547A=	NP_001243502.1:p.Lys183=
NR_046317.2:n.1284A=
NM_000744.7:c.1075A= MANE Select	NP_000735.1:p.Lys359=