Canonical Allele Identifier: CA2374743229

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350915T= , CM000682.2:g.63350915T=	GRCh38
NC_000020.10:g.61982267T= , CM000682.1:g.61982267T=	GRCh37
NC_000020.9:g.61452711T=	NCBI36
NG_011931.1:g.15429A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.496A= MANE Select	ENSP00000359285.4:p.Thr166=
ENST00000370263.8:c.496A=	ENSP00000359285.4:p.Thr166=
ENST00000463705.5:n.1144A=
ENST00000467563.3:n.566A=
ENST00000498043.6:c.520A=
ENST00000615287.4:c.283A=	ENSP00000483388.1:p.Thr95=
ENST00000627000.1:c.*185A=	ENSP00000486914.1:n.*185A=
ENST00000628665.1:n.539A=
ENST00000630240.1:n.217A=
NM_000744.6:c.496A=	NP_000735.1:p.Thr166=
NM_001256573.1:c.-33A=	NP_001243502.1:n.-33A=
NR_046317.1:n.752A=
XM_011528524.1:c.283A=	XP_011526826.1:p.Thr95=
XM_017027625.2:c.-33A=	XP_016883114.1:n.-33A=
XM_024451822.1:c.-33A=	XP_024307590.1:n.-33A=
NM_001256573.2:c.-33A=	NP_001243502.1:n.-33A=
NR_046317.2:n.705A=
NM_000744.7:c.496A= MANE Select	NP_000735.1:p.Thr166=