Canonical Allele Identifier: CA2374743067

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350617A= , CM000682.2:g.63350617A=	GRCh38
NC_000020.10:g.61981969A= , CM000682.1:g.61981969A=	GRCh37
NC_000020.9:g.61452413A=	NCBI36
NG_011931.1:g.15727T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.794T= MANE Select	ENSP00000359285.4:p.Phe265=
ENST00000370263.8:c.794T=	ENSP00000359285.4:p.Phe265=
ENST00000463705.5:n.1442T=
ENST00000467563.3:n.864T=
ENST00000498043.6:c.818T=
ENST00000615287.4:c.581T=	ENSP00000483388.1:p.Phe194=
ENST00000627000.1:c.*483T=	ENSP00000486914.1:n.*483T=
ENST00000630240.1:n.515T=
NM_000744.6:c.794T=	NP_000735.1:p.Phe265=
NM_001256573.1:c.266T=	NP_001243502.1:p.Phe89=
NR_046317.1:n.1050T=
XM_011528524.1:c.581T=	XP_011526826.1:p.Phe194=
XM_017027625.2:c.266T=	XP_016883114.1:p.Phe89=
XM_024451822.1:c.266T=	XP_024307590.1:p.Phe89=
NM_001256573.2:c.266T=	NP_001243502.1:p.Phe89=
NR_046317.2:n.1003T=
NM_000744.7:c.794T= MANE Select	NP_000735.1:p.Phe265=