Canonical Allele Identifier: CA2374743211

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350885T= , CM000682.2:g.63350885T=	GRCh38
NC_000020.10:g.61982237T= , CM000682.1:g.61982237T=	GRCh37
NC_000020.9:g.61452681T=	NCBI36
NG_011931.1:g.15459A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.526A= MANE Select	ENSP00000359285.4:p.Thr176=
ENST00000370263.8:c.526A=	ENSP00000359285.4:p.Thr176=
ENST00000463705.5:n.1174A=
ENST00000467563.3:n.596A=
ENST00000498043.6:c.550A=
ENST00000615287.4:c.313A=	ENSP00000483388.1:p.Thr105=
ENST00000627000.1:c.*215A=	ENSP00000486914.1:n.*215A=
ENST00000630240.1:n.247A=
NM_000744.6:c.526A=	NP_000735.1:p.Thr176=
NM_001256573.1:c.-3A=	NP_001243502.1:n.-3A=
NR_046317.1:n.782A=
XM_011528524.1:c.313A=	XP_011526826.1:p.Thr105=
XM_017027625.2:c.-3A=	XP_016883114.1:n.-3A=
XM_024451822.1:c.-3A=	XP_024307590.1:n.-3A=
NM_001256573.2:c.-3A=	NP_001243502.1:n.-3A=
NR_046317.2:n.735A=
NM_000744.7:c.526A= MANE Select	NP_000735.1:p.Thr176=