Canonical Allele Identifier: CA2374743027
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350540G= , CM000682.2:g.63350540G= GRCh38
NC_000020.10:g.61981892G= , CM000682.1:g.61981892G= GRCh37
NC_000020.9:g.61452336G= NCBI36
NG_011931.1:g.15804C=

Transcript Alleles

HGVS Amino-acid change
ENST00000370263.9:c.871C= MANE Select ENSP00000359285.4:p.Leu291=
ENST00000370263.8:c.871C= ENSP00000359285.4:p.Leu291=
ENST00000463705.5:n.1519C=
ENST00000467563.3:n.941C=
ENST00000498043.6:c.895C=
ENST00000615287.4:c.658C= ENSP00000483388.1:p.Leu220=
ENST00000627000.1:c.*560C= ENSP00000486914.1:n.*560C=
ENST00000630240.1:n.592C=
NM_000744.6:c.871C= NP_000735.1:p.Leu291=
NM_001256573.1:c.343C= NP_001243502.1:p.Leu115=
NR_046317.1:n.1127C=
XM_011528524.1:c.658C= XP_011526826.1:p.Leu220=
XM_017027625.2:c.343C= XP_016883114.1:p.Leu115=
XM_024451822.1:c.343C= XP_024307590.1:p.Leu115=
NM_001256573.2:c.343C= NP_001243502.1:p.Leu115=
NR_046317.2:n.1080C=
NM_000744.7:c.871C= MANE Select NP_000735.1:p.Leu291=