Canonical Allele Identifier: CA2374743000

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350495T= , CM000682.2:g.63350495T=	GRCh38
NC_000020.10:g.61981847T= , CM000682.1:g.61981847T=	GRCh37
NC_000020.9:g.61452291T=	NCBI36
NG_011931.1:g.15849A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.916A= MANE Select	ENSP00000359285.4:p.Ile306=
ENST00000370263.8:c.916A=	ENSP00000359285.4:p.Ile306=
ENST00000463705.5:n.1564A=
ENST00000467563.3:n.986A=
ENST00000498043.6:c.940A=
ENST00000615287.4:c.703A=	ENSP00000483388.1:p.Ile235=
ENST00000627000.1:c.*605A=	ENSP00000486914.1:n.*605A=
ENST00000630240.1:n.637A=
NM_000744.6:c.916A=	NP_000735.1:p.Ile306=
NM_001256573.1:c.388A=	NP_001243502.1:p.Ile130=
NR_046317.1:n.1172A=
XM_011528524.1:c.703A=	XP_011526826.1:p.Ile235=
XM_017027625.2:c.388A=	XP_016883114.1:p.Ile130=
XM_024451822.1:c.388A=	XP_024307590.1:p.Ile130=
NM_001256573.2:c.388A=	NP_001243502.1:p.Ile130=
NR_046317.2:n.1125A=
NM_000744.7:c.916A= MANE Select	NP_000735.1:p.Ile306=