Canonical Allele Identifier: CA2842938882

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349717dup , CM000682.2:g.63349717dup	GRCh38
NC_000020.10:g.61981069dup , CM000682.1:g.61981069dup	GRCh37
NC_000020.9:g.61451513dup	NCBI36
NG_011931.1:g.16629dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1696dup MANE Select	ENSP00000359285.4:p.Arg566ProfsTer?
ENST00000370263.8:c.1696dup	ENSP00000359285.4:p.Arg566ProfsTer?
ENST00000463705.5:n.2344dup
ENST00000467563.3:n.1766dup
ENST00000498043.6:c.1720dup
ENST00000615287.4:c.1483dup	ENSP00000483388.1:p.Arg495ProfsTer?
ENST00000627000.1:c.*1385dup	ENSP00000486914.1:n.*1385dup
ENST00000630240.1:n.1417dup
NM_000744.6:c.1696dup	NP_000735.1:p.Arg566ProfsTer?
NM_001256573.1:c.1168dup	NP_001243502.1:p.Arg390ProfsTer?
NR_046317.1:n.1952dup
XM_011528524.1:c.1483dup	XP_011526826.1:p.Arg495ProfsTer?
XM_017027625.2:c.1168dup	XP_016883114.1:p.Arg390ProfsTer?
XM_024451822.1:c.1168dup	XP_024307590.1:p.Arg390ProfsTer?
NM_001256573.2:c.1168dup	NP_001243502.1:p.Arg390ProfsTer?
NR_046317.2:n.1905dup
NM_000744.7:c.1696dup MANE Select	NP_000735.1:p.Arg566ProfsTer?