Canonical Allele Identifier: CA9957716
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 661894
dbSNP Id: rs764238999

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350570C>T , CM000682.2:g.63350570C>T GRCh38
NC_000020.10:g.61981922C>T , CM000682.1:g.61981922C>T GRCh37
NC_000020.9:g.61452366C>T NCBI36
NG_011931.1:g.15774G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.841G>A MANE Select ENSP00000359285.4:p.Val281Met
ENST00000370263.8:c.841G>A ENSP00000359285.4:p.Val281Met
ENST00000463705.5:n.1489G>A
ENST00000467563.3:n.911G>A
ENST00000498043.6:c.865G>A
ENST00000615287.4:c.628G>A ENSP00000483388.1:p.Val210Met
ENST00000627000.1:c.*530G>A ENSP00000486914.1:n.*530G>A
ENST00000630240.1:n.562G>A
NM_000744.6:c.841G>A NP_000735.1:p.Val281Met
NM_001256573.1:c.313G>A NP_001243502.1:p.Val105Met
NR_046317.1:n.1097G>A
XM_011528524.1:c.628G>A XP_011526826.1:p.Val210Met
XM_017027625.2:c.313G>A XP_016883114.1:p.Val105Met
XM_024451822.1:c.313G>A XP_024307590.1:p.Val105Met
NM_001256573.2:c.313G>A NP_001243502.1:p.Val105Met
NR_046317.2:n.1050G>A
NM_000744.7:c.841G>A MANE Select NP_000735.1:p.Val281Met