Canonical Allele Identifier: CA409638055

Gene: CHRNA4

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350867A>T , CM000682.2:g.63350867A>T	GRCh38
NC_000020.10:g.61982219A>T , CM000682.1:g.61982219A>T	GRCh37
NC_000020.9:g.61452663A>T	NCBI36
NG_011931.1:g.15477T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.544T>A MANE Select	ENSP00000359285.4:p.Trp182Arg
ENST00000370263.8:c.544T>A	ENSP00000359285.4:p.Trp182Arg
ENST00000463705.5:n.1192T>A
ENST00000467563.3:n.614T>A
ENST00000498043.6:c.568T>A
ENST00000615287.4:c.331T>A	ENSP00000483388.1:p.Trp111Arg
ENST00000627000.1:c.*233T>A	ENSP00000486914.1:n.*233T>A
ENST00000630240.1:n.265T>A
NM_000744.6:c.544T>A	NP_000735.1:p.Trp182Arg
NM_001256573.1:c.16T>A	NP_001243502.1:p.Trp6Arg
NR_046317.1:n.800T>A
XM_011528524.1:c.331T>A	XP_011526826.1:p.Trp111Arg
XM_017027625.2:c.16T>A	XP_016883114.1:p.Trp6Arg
XM_024451822.1:c.16T>A	XP_024307590.1:p.Trp6Arg
NM_001256573.2:c.16T>A	NP_001243502.1:p.Trp6Arg
NR_046317.2:n.753T>A
NM_000744.7:c.544T>A MANE Select	NP_000735.1:p.Trp182Arg