Canonical Allele Identifier: CA2374743147

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350753T= , CM000682.2:g.63350753T=	GRCh38
NC_000020.10:g.61982105T= , CM000682.1:g.61982105T=	GRCh37
NC_000020.9:g.61452549T=	NCBI36
NG_011931.1:g.15591A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.658A= MANE Select	ENSP00000359285.4:p.Thr220=
ENST00000370263.8:c.658A=	ENSP00000359285.4:p.Thr220=
ENST00000463705.5:n.1306A=
ENST00000467563.3:n.728A=
ENST00000498043.6:c.682A=
ENST00000615287.4:c.445A=	ENSP00000483388.1:p.Thr149=
ENST00000627000.1:c.*347A=	ENSP00000486914.1:n.*347A=
ENST00000630240.1:n.379A=
NM_000744.6:c.658A=	NP_000735.1:p.Thr220=
NM_001256573.1:c.130A=	NP_001243502.1:p.Thr44=
NR_046317.1:n.914A=
XM_011528524.1:c.445A=	XP_011526826.1:p.Thr149=
XM_017027625.2:c.130A=	XP_016883114.1:p.Thr44=
XM_024451822.1:c.130A=	XP_024307590.1:p.Thr44=
NM_001256573.2:c.130A=	NP_001243502.1:p.Thr44=
NR_046317.2:n.867A=
NM_000744.7:c.658A= MANE Select	NP_000735.1:p.Thr220=