Canonical Allele Identifier: CA2374742977
Gene: CHRNA4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63350454C= , CM000682.2:g.63350454C= GRCh38
NC_000020.10:g.61981806C= , CM000682.1:g.61981806C= GRCh37
NC_000020.9:g.61452250C= NCBI36
NG_011931.1:g.15890G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370263.9:c.957G= MANE Select ENSP00000359285.4:p.Leu319=
ENST00000370263.8:c.957G= ENSP00000359285.4:p.Leu319=
ENST00000463705.5:n.1605G=
ENST00000467563.3:n.1027G=
ENST00000498043.6:c.981G=
ENST00000615287.4:c.744G= ENSP00000483388.1:p.Leu248=
ENST00000627000.1:c.*646G= ENSP00000486914.1:n.*646G=
ENST00000630240.1:n.678G=
NM_000744.6:c.957G= NP_000735.1:p.Leu319=
NM_001256573.1:c.429G= NP_001243502.1:p.Leu143=
NR_046317.1:n.1213G=
XM_011528524.1:c.744G= XP_011526826.1:p.Leu248=
XM_017027625.2:c.429G= XP_016883114.1:p.Leu143=
XM_024451822.1:c.429G= XP_024307590.1:p.Leu143=
NM_001256573.2:c.429G= NP_001243502.1:p.Leu143=
NR_046317.2:n.1166G=
NM_000744.7:c.957G= MANE Select NP_000735.1:p.Leu319=