Canonical Allele Identifier: CA2374743214
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350890T= , CM000682.2:g.63350890T= GRCh38
NC_000020.10:g.61982242T= , CM000682.1:g.61982242T= GRCh37
NC_000020.9:g.61452686T= NCBI36
NG_011931.1:g.15454A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.521A= MANE Select ENSP00000359285.4:p.Asn174=
ENST00000370263.8:c.521A= ENSP00000359285.4:p.Asn174=
ENST00000463705.5:n.1169A=
ENST00000467563.3:n.591A=
ENST00000498043.6:c.545A=
ENST00000615287.4:c.308A= ENSP00000483388.1:p.Asn103=
ENST00000627000.1:c.*210A= ENSP00000486914.1:n.*210A=
ENST00000630240.1:n.242A=
NM_000744.6:c.521A= NP_000735.1:p.Asn174=
NM_001256573.1:c.-8A= NP_001243502.1:n.-8A=
NR_046317.1:n.777A=
XM_011528524.1:c.308A= XP_011526826.1:p.Asn103=
XM_017027625.2:c.-8A= XP_016883114.1:n.-8A=
XM_024451822.1:c.-8A= XP_024307590.1:n.-8A=
NM_001256573.2:c.-8A= NP_001243502.1:n.-8A=
NR_046317.2:n.730A=
NM_000744.7:c.521A= MANE Select NP_000735.1:p.Asn174=