Canonical Allele Identifier: CA2374743182

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350819C= , CM000682.2:g.63350819C=	GRCh38
NC_000020.10:g.61982171C= , CM000682.1:g.61982171C=	GRCh37
NC_000020.9:g.61452615C=	NCBI36
NG_011931.1:g.15525G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.592G= MANE Select	ENSP00000359285.4:p.Val198=
ENST00000370263.8:c.592G=	ENSP00000359285.4:p.Val198=
ENST00000463705.5:n.1240G=
ENST00000467563.3:n.662G=
ENST00000498043.6:c.616G=
ENST00000615287.4:c.379G=	ENSP00000483388.1:p.Val127=
ENST00000627000.1:c.*281G=	ENSP00000486914.1:n.*281G=
ENST00000630240.1:n.313G=
NM_000744.6:c.592G=	NP_000735.1:p.Val198=
NM_001256573.1:c.64G=	NP_001243502.1:p.Val22=
NR_046317.1:n.848G=
XM_011528524.1:c.379G=	XP_011526826.1:p.Val127=
XM_017027625.2:c.64G=	XP_016883114.1:p.Val22=
XM_024451822.1:c.64G=	XP_024307590.1:p.Val22=
NM_001256573.2:c.64G=	NP_001243502.1:p.Val22=
NR_046317.2:n.801G=
NM_000744.7:c.592G= MANE Select	NP_000735.1:p.Val198=