Canonical Allele Identifier: CA2374743208
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350873C= , CM000682.2:g.63350873C= GRCh38
NC_000020.10:g.61982225C= , CM000682.1:g.61982225C= GRCh37
NC_000020.9:g.61452669C= NCBI36
NG_011931.1:g.15471G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.538G= MANE Select ENSP00000359285.4:p.Gly180=
ENST00000370263.8:c.538G= ENSP00000359285.4:p.Gly180=
ENST00000463705.5:n.1186G=
ENST00000467563.3:n.608G=
ENST00000498043.6:c.562G=
ENST00000615287.4:c.325G= ENSP00000483388.1:p.Gly109=
ENST00000627000.1:c.*227G= ENSP00000486914.1:n.*227G=
ENST00000630240.1:n.259G=
NM_000744.6:c.538G= NP_000735.1:p.Gly180=
NM_001256573.1:c.10G= NP_001243502.1:p.Gly4=
NR_046317.1:n.794G=
XM_011528524.1:c.325G= XP_011526826.1:p.Gly109=
XM_017027625.2:c.10G= XP_016883114.1:p.Gly4=
XM_024451822.1:c.10G= XP_024307590.1:p.Gly4=
NM_001256573.2:c.10G= NP_001243502.1:p.Gly4=
NR_046317.2:n.747G=
NM_000744.7:c.538G= MANE Select NP_000735.1:p.Gly180=