Canonical Allele Identifier: CA2374743017

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350525T= , CM000682.2:g.63350525T=	GRCh38
NC_000020.10:g.61981877T= , CM000682.1:g.61981877T=	GRCh37
NC_000020.9:g.61452321T=	NCBI36
NG_011931.1:g.15819A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.886A= MANE Select	ENSP00000359285.4:p.Ile296=
ENST00000370263.8:c.886A=	ENSP00000359285.4:p.Ile296=
ENST00000463705.5:n.1534A=
ENST00000467563.3:n.956A=
ENST00000498043.6:c.910A=
ENST00000615287.4:c.673A=	ENSP00000483388.1:p.Ile225=
ENST00000627000.1:c.*575A=	ENSP00000486914.1:n.*575A=
ENST00000630240.1:n.607A=
NM_000744.6:c.886A=	NP_000735.1:p.Ile296=
NM_001256573.1:c.358A=	NP_001243502.1:p.Ile120=
NR_046317.1:n.1142A=
XM_011528524.1:c.673A=	XP_011526826.1:p.Ile225=
XM_017027625.2:c.358A=	XP_016883114.1:p.Ile120=
XM_024451822.1:c.358A=	XP_024307590.1:p.Ile120=
NM_001256573.2:c.358A=	NP_001243502.1:p.Ile120=
NR_046317.2:n.1095A=
NM_000744.7:c.886A= MANE Select	NP_000735.1:p.Ile296=