Canonical Allele Identifier: CA2374742523

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349697G= , CM000682.2:g.63349697G=	GRCh38
NC_000020.10:g.61981049G= , CM000682.1:g.61981049G=	GRCh37
NC_000020.9:g.61451493G=	NCBI36
NG_011931.1:g.16647C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1714C= MANE Select	ENSP00000359285.4:p.Gln572=
ENST00000370263.8:c.1714C=	ENSP00000359285.4:p.Gln572=
ENST00000463705.5:n.2362C=
ENST00000467563.3:n.1784C=
ENST00000498043.6:c.1738C=
ENST00000615287.4:c.1501C=	ENSP00000483388.1:p.Gln501=
ENST00000627000.1:c.*1403C=	ENSP00000486914.1:n.*1403C=
ENST00000630240.1:n.1435C=
NM_000744.6:c.1714C=	NP_000735.1:p.Gln572=
NM_001256573.1:c.1186C=	NP_001243502.1:p.Gln396=
NR_046317.1:n.1970C=
XM_011528524.1:c.1501C=	XP_011526826.1:p.Gln501=
XM_017027625.2:c.1186C=	XP_016883114.1:p.Gln396=
XM_024451822.1:c.1186C=	XP_024307590.1:p.Gln396=
NM_001256573.2:c.1186C=	NP_001243502.1:p.Gln396=
NR_046317.2:n.1923C=
NM_000744.7:c.1714C= MANE Select	NP_000735.1:p.Gln572=