Canonical Allele Identifier: CA409638176
Gene: CHRNA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350892C>A , CM000682.2:g.63350892C>A GRCh38
NC_000020.10:g.61982244C>A , CM000682.1:g.61982244C>A GRCh37
NC_000020.9:g.61452688C>A NCBI36
NG_011931.1:g.15452G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.519G>T MANE Select ENSP00000359285.4:p.Gln173His
ENST00000370263.8:c.519G>T ENSP00000359285.4:p.Gln173His
ENST00000463705.5:n.1167G>T
ENST00000467563.3:n.589G>T
ENST00000498043.6:c.543G>T
ENST00000615287.4:c.306G>T ENSP00000483388.1:p.Gln102His
ENST00000627000.1:c.*208G>T ENSP00000486914.1:n.*208G>T
ENST00000630240.1:n.240G>T
NM_000744.6:c.519G>T NP_000735.1:p.Gln173His
NM_001256573.1:c.-10G>T NP_001243502.1:n.-10G>T
NR_046317.1:n.775G>T
XM_011528524.1:c.306G>T XP_011526826.1:p.Gln102His
XM_017027625.2:c.-10G>T XP_016883114.1:n.-10G>T
XM_024451822.1:c.-10G>T XP_024307590.1:n.-10G>T
NM_001256573.2:c.-10G>T NP_001243502.1:n.-10G>T
NR_046317.2:n.728G>T
NM_000744.7:c.519G>T MANE Select NP_000735.1:p.Gln173His