Canonical Allele Identifier: CA409637041
Gene: CHRNA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350699C>A , CM000682.2:g.63350699C>A GRCh38
NC_000020.10:g.61982051C>A , CM000682.1:g.61982051C>A GRCh37
NC_000020.9:g.61452495C>A NCBI36
NG_011931.1:g.15645G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.712G>T MANE Select ENSP00000359285.4:p.Val238Phe
ENST00000370263.8:c.712G>T ENSP00000359285.4:p.Val238Phe
ENST00000463705.5:n.1360G>T
ENST00000467563.3:n.782G>T
ENST00000498043.6:c.736G>T
ENST00000615287.4:c.499G>T ENSP00000483388.1:p.Val167Phe
ENST00000627000.1:c.*401G>T ENSP00000486914.1:n.*401G>T
ENST00000630240.1:n.433G>T
NM_000744.6:c.712G>T NP_000735.1:p.Val238Phe
NM_001256573.1:c.184G>T NP_001243502.1:p.Val62Phe
NR_046317.1:n.968G>T
XM_011528524.1:c.499G>T XP_011526826.1:p.Val167Phe
XM_017027625.2:c.184G>T XP_016883114.1:p.Val62Phe
XM_024451822.1:c.184G>T XP_024307590.1:p.Val62Phe
NM_001256573.2:c.184G>T NP_001243502.1:p.Val62Phe
NR_046317.2:n.921G>T
NM_000744.7:c.712G>T MANE Select NP_000735.1:p.Val238Phe