Canonical Allele Identifier: CA2374743050

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350588T= , CM000682.2:g.63350588T=	GRCh38
NC_000020.10:g.61981940T= , CM000682.1:g.61981940T=	GRCh37
NC_000020.9:g.61452384T=	NCBI36
NG_011931.1:g.15756A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.823A= MANE Select	ENSP00000359285.4:p.Ile275=
ENST00000370263.8:c.823A=	ENSP00000359285.4:p.Ile275=
ENST00000463705.5:n.1471A=
ENST00000467563.3:n.893A=
ENST00000498043.6:c.847A=
ENST00000615287.4:c.610A=	ENSP00000483388.1:p.Ile204=
ENST00000627000.1:c.*512A=	ENSP00000486914.1:n.*512A=
ENST00000630240.1:n.544A=
NM_000744.6:c.823A=	NP_000735.1:p.Ile275=
NM_001256573.1:c.295A=	NP_001243502.1:p.Ile99=
NR_046317.1:n.1079A=
XM_011528524.1:c.610A=	XP_011526826.1:p.Ile204=
XM_017027625.2:c.295A=	XP_016883114.1:p.Ile99=
XM_024451822.1:c.295A=	XP_024307590.1:p.Ile99=
NM_001256573.2:c.295A=	NP_001243502.1:p.Ile99=
NR_046317.2:n.1032A=
NM_000744.7:c.823A= MANE Select	NP_000735.1:p.Ile275=