Canonical Allele Identifier: CA409636368
Gene: CHRNA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350528T>A , CM000682.2:g.63350528T>A GRCh38
NC_000020.10:g.61981880T>A , CM000682.1:g.61981880T>A GRCh37
NC_000020.9:g.61452324T>A NCBI36
NG_011931.1:g.15816A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.883A>T MANE Select ENSP00000359285.4:p.Ile295Phe
ENST00000370263.8:c.883A>T ENSP00000359285.4:p.Ile295Phe
ENST00000463705.5:n.1531A>T
ENST00000467563.3:n.953A>T
ENST00000498043.6:c.907A>T
ENST00000615287.4:c.670A>T ENSP00000483388.1:p.Ile224Phe
ENST00000627000.1:c.*572A>T ENSP00000486914.1:n.*572A>T
ENST00000630240.1:n.604A>T
NM_000744.6:c.883A>T NP_000735.1:p.Ile295Phe
NM_001256573.1:c.355A>T NP_001243502.1:p.Ile119Phe
NR_046317.1:n.1139A>T
XM_011528524.1:c.670A>T XP_011526826.1:p.Ile224Phe
XM_017027625.2:c.355A>T XP_016883114.1:p.Ile119Phe
XM_024451822.1:c.355A>T XP_024307590.1:p.Ile119Phe
NM_001256573.2:c.355A>T NP_001243502.1:p.Ile119Phe
NR_046317.2:n.1092A>T
NM_000744.7:c.883A>T MANE Select NP_000735.1:p.Ile295Phe