Canonical Allele Identifier: CA9957660
Gene: CHRNA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1086721
ClinVar RCV Id: RCV001404562
dbSNP Id: rs74396179

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350325G>A , CM000682.2:g.63350325G>A GRCh38
NC_000020.10:g.61981677G>A , CM000682.1:g.61981677G>A GRCh37
NC_000020.9:g.61452121G>A NCBI36
NG_011931.1:g.16019C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.1086C>T MANE Select ENSP00000359285.4:p.Ser362=
ENST00000370263.8:c.1086C>T ENSP00000359285.4:p.Ser362=
ENST00000463705.5:n.1734C>T
ENST00000467563.3:n.1156C>T
ENST00000498043.6:c.1110C>T
ENST00000615287.4:c.873C>T ENSP00000483388.1:p.Ser291=
ENST00000627000.1:c.*775C>T ENSP00000486914.1:n.*775C>T
ENST00000630240.1:n.807C>T
NM_000744.6:c.1086C>T NP_000735.1:p.Ser362=
NM_001256573.1:c.558C>T NP_001243502.1:p.Ser186=
NR_046317.1:n.1342C>T
XM_011528524.1:c.873C>T XP_011526826.1:p.Ser291=
XM_017027625.2:c.558C>T XP_016883114.1:p.Ser186=
XM_024451822.1:c.558C>T XP_024307590.1:p.Ser186=
NM_001256573.2:c.558C>T NP_001243502.1:p.Ser186=
NR_046317.2:n.1295C>T
NM_000744.7:c.1086C>T MANE Select NP_000735.1:p.Ser362=