Canonical Allele Identifier: CA2374743233

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350921C= , CM000682.2:g.63350921C=	GRCh38
NC_000020.10:g.61982273C= , CM000682.1:g.61982273C=	GRCh37
NC_000020.9:g.61452717C=	NCBI36
NG_011931.1:g.15423G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.490G= MANE Select	ENSP00000359285.4:p.Asp164=
ENST00000370263.8:c.490G=	ENSP00000359285.4:p.Asp164=
ENST00000463705.5:n.1138G=
ENST00000467563.3:n.560G=
ENST00000498043.6:c.514G=
ENST00000615287.4:c.277G=	ENSP00000483388.1:p.Asp93=
ENST00000627000.1:c.*179G=	ENSP00000486914.1:n.*179G=
ENST00000628665.1:n.533G=
ENST00000630240.1:n.211G=
NM_000744.6:c.490G=	NP_000735.1:p.Asp164=
NM_001256573.1:c.-39G=	NP_001243502.1:n.-39G=
NR_046317.1:n.746G=
XM_011528524.1:c.277G=	XP_011526826.1:p.Asp93=
XM_017027625.2:c.-39G=	XP_016883114.1:n.-39G=
XM_024451822.1:c.-39G=	XP_024307590.1:n.-39G=
NM_001256573.2:c.-39G=	NP_001243502.1:n.-39G=
NR_046317.2:n.699G=
NM_000744.7:c.490G= MANE Select	NP_000735.1:p.Asp164=