Canonical Allele Identifier: CA2374743221

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350901G= , CM000682.2:g.63350901G=	GRCh38
NC_000020.10:g.61982253G= , CM000682.1:g.61982253G=	GRCh37
NC_000020.9:g.61452697G=	NCBI36
NG_011931.1:g.15443C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.510C= MANE Select	ENSP00000359285.4:p.Phe170=
ENST00000370263.8:c.510C=	ENSP00000359285.4:p.Phe170=
ENST00000463705.5:n.1158C=
ENST00000467563.3:n.580C=
ENST00000498043.6:c.534C=
ENST00000615287.4:c.297C=	ENSP00000483388.1:p.Phe99=
ENST00000627000.1:c.*199C=	ENSP00000486914.1:n.*199C=
ENST00000630240.1:n.231C=
NM_000744.6:c.510C=	NP_000735.1:p.Phe170=
NM_001256573.1:c.-19C=	NP_001243502.1:n.-19C=
NR_046317.1:n.766C=
XM_011528524.1:c.297C=	XP_011526826.1:p.Phe99=
XM_017027625.2:c.-19C=	XP_016883114.1:n.-19C=
XM_024451822.1:c.-19C=	XP_024307590.1:n.-19C=
NM_001256573.2:c.-19C=	NP_001243502.1:n.-19C=
NR_046317.2:n.719C=
NM_000744.7:c.510C= MANE Select	NP_000735.1:p.Phe170=