Canonical Allele Identifier: CA2374743219

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350898G= , CM000682.2:g.63350898G=	GRCh38
NC_000020.10:g.61982250G= , CM000682.1:g.61982250G=	GRCh37
NC_000020.9:g.61452694G=	NCBI36
NG_011931.1:g.15446C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.513C= MANE Select	ENSP00000359285.4:p.Asp171=
ENST00000370263.8:c.513C=	ENSP00000359285.4:p.Asp171=
ENST00000463705.5:n.1161C=
ENST00000467563.3:n.583C=
ENST00000498043.6:c.537C=
ENST00000615287.4:c.300C=	ENSP00000483388.1:p.Asp100=
ENST00000627000.1:c.*202C=	ENSP00000486914.1:n.*202C=
ENST00000630240.1:n.234C=
NM_000744.6:c.513C=	NP_000735.1:p.Asp171=
NM_001256573.1:c.-16C=	NP_001243502.1:n.-16C=
NR_046317.1:n.769C=
XM_011528524.1:c.300C=	XP_011526826.1:p.Asp100=
XM_017027625.2:c.-16C=	XP_016883114.1:n.-16C=
XM_024451822.1:c.-16C=	XP_024307590.1:n.-16C=
NM_001256573.2:c.-16C=	NP_001243502.1:n.-16C=
NR_046317.2:n.722C=
NM_000744.7:c.513C= MANE Select	NP_000735.1:p.Asp171=