Canonical Allele Identifier: CA2374743169

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350786A= , CM000682.2:g.63350786A=	GRCh38
NC_000020.10:g.61982138A= , CM000682.1:g.61982138A=	GRCh37
NC_000020.9:g.61452582A=	NCBI36
NG_011931.1:g.15558T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.625T= MANE Select	ENSP00000359285.4:p.Trp209=
ENST00000370263.8:c.625T=	ENSP00000359285.4:p.Trp209=
ENST00000463705.5:n.1273T=
ENST00000467563.3:n.695T=
ENST00000498043.6:c.649T=
ENST00000615287.4:c.412T=	ENSP00000483388.1:p.Trp138=
ENST00000627000.1:c.*314T=	ENSP00000486914.1:n.*314T=
ENST00000630240.1:n.346T=
NM_000744.6:c.625T=	NP_000735.1:p.Trp209=
NM_001256573.1:c.97T=	NP_001243502.1:p.Trp33=
NR_046317.1:n.881T=
XM_011528524.1:c.412T=	XP_011526826.1:p.Trp138=
XM_017027625.2:c.97T=	XP_016883114.1:p.Trp33=
XM_024451822.1:c.97T=	XP_024307590.1:p.Trp33=
NM_001256573.2:c.97T=	NP_001243502.1:p.Trp33=
NR_046317.2:n.834T=
NM_000744.7:c.625T= MANE Select	NP_000735.1:p.Trp209=