Canonical Allele Identifier: CA2374742625
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63349883G= , CM000682.2:g.63349883G= GRCh38
NC_000020.10:g.61981235G= , CM000682.1:g.61981235G= GRCh37
NC_000020.9:g.61451679G= NCBI36
NG_011931.1:g.16461C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.1528C= MANE Select ENSP00000359285.4:p.Leu510=
ENST00000370263.8:c.1528C= ENSP00000359285.4:p.Leu510=
ENST00000463705.5:n.2176C=
ENST00000467563.3:n.1598C=
ENST00000498043.6:c.1552C=
ENST00000615287.4:c.1315C= ENSP00000483388.1:p.Leu439=
ENST00000627000.1:c.*1217C= ENSP00000486914.1:n.*1217C=
ENST00000630240.1:n.1249C=
NM_000744.6:c.1528C= NP_000735.1:p.Leu510=
NM_001256573.1:c.1000C= NP_001243502.1:p.Leu334=
NR_046317.1:n.1784C=
XM_011528524.1:c.1315C= XP_011526826.1:p.Leu439=
XM_017027625.2:c.1000C= XP_016883114.1:p.Leu334=
XM_024451822.1:c.1000C= XP_024307590.1:p.Leu334=
NM_001256573.2:c.1000C= NP_001243502.1:p.Leu334=
NR_046317.2:n.1737C=
NM_000744.7:c.1528C= MANE Select NP_000735.1:p.Leu510=