Canonical Allele Identifier: CA2374743228

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350912A= , CM000682.2:g.63350912A=	GRCh38
NC_000020.10:g.61982264A= , CM000682.1:g.61982264A=	GRCh37
NC_000020.9:g.61452708A=	NCBI36
NG_011931.1:g.15432T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.499T= MANE Select	ENSP00000359285.4:p.Phe167=
ENST00000370263.8:c.499T=	ENSP00000359285.4:p.Phe167=
ENST00000463705.5:n.1147T=
ENST00000467563.3:n.569T=
ENST00000498043.6:c.523T=
ENST00000615287.4:c.286T=	ENSP00000483388.1:p.Phe96=
ENST00000627000.1:c.*188T=	ENSP00000486914.1:n.*188T=
ENST00000628665.1:n.542T=
ENST00000630240.1:n.220T=
NM_000744.6:c.499T=	NP_000735.1:p.Phe167=
NM_001256573.1:c.-30T=	NP_001243502.1:n.-30T=
NR_046317.1:n.755T=
XM_011528524.1:c.286T=	XP_011526826.1:p.Phe96=
XM_017027625.2:c.-30T=	XP_016883114.1:n.-30T=
XM_024451822.1:c.-30T=	XP_024307590.1:n.-30T=
NM_001256573.2:c.-30T=	NP_001243502.1:n.-30T=
NR_046317.2:n.708T=
NM_000744.7:c.499T= MANE Select	NP_000735.1:p.Phe167=