Canonical Allele Identifier: CA343925
Gene: CHRNA4 HGNC NCBI

Linked Data

dbSNP Id: rs281865066

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350533G>A , CM000682.2:g.63350533G>A GRCh38
NC_000020.10:g.61981885G>A , CM000682.1:g.61981885G>A GRCh37
NC_000020.9:g.61452329G>A NCBI36
NG_011931.1:g.15811C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000370263.9:c.878C>T MANE Select ENSP00000359285.4:p.Thr293Ile
ENST00000370263.8:c.878C>T ENSP00000359285.4:p.Thr293Ile
ENST00000463705.5:n.1526C>T
ENST00000467563.3:n.948C>T
ENST00000498043.6:c.902C>T
ENST00000615287.4:c.665C>T ENSP00000483388.1:p.Thr222Ile
ENST00000627000.1:c.*567C>T ENSP00000486914.1:n.*567C>T
ENST00000630240.1:n.599C>T
NM_000744.6:c.878C>T NP_000735.1:p.Thr293Ile
NM_001256573.1:c.350C>T NP_001243502.1:p.Thr117Ile
NR_046317.1:n.1134C>T
XM_011528524.1:c.665C>T XP_011526826.1:p.Thr222Ile
XM_017027625.2:c.350C>T XP_016883114.1:p.Thr117Ile
XM_024451822.1:c.350C>T XP_024307590.1:p.Thr117Ile
NM_001256573.2:c.350C>T NP_001243502.1:p.Thr117Ile
NR_046317.2:n.1087C>T
NM_000744.7:c.878C>T MANE Select NP_000735.1:p.Thr293Ile