Canonical Allele Identifier: CA2374743008

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350508C= , CM000682.2:g.63350508C=	GRCh38
NC_000020.10:g.61981860C= , CM000682.1:g.61981860C=	GRCh37
NC_000020.9:g.61452304C=	NCBI36
NG_011931.1:g.15836G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.903G= MANE Select	ENSP00000359285.4:p.Leu301=
ENST00000370263.8:c.903G=	ENSP00000359285.4:p.Leu301=
ENST00000463705.5:n.1551G=
ENST00000467563.3:n.973G=
ENST00000498043.6:c.927G=
ENST00000615287.4:c.690G=	ENSP00000483388.1:p.Leu230=
ENST00000627000.1:c.*592G=	ENSP00000486914.1:n.*592G=
ENST00000630240.1:n.624G=
NM_000744.6:c.903G=	NP_000735.1:p.Leu301=
NM_001256573.1:c.375G=	NP_001243502.1:p.Leu125=
NR_046317.1:n.1159G=
XM_011528524.1:c.690G=	XP_011526826.1:p.Leu230=
XM_017027625.2:c.375G=	XP_016883114.1:p.Leu125=
XM_024451822.1:c.375G=	XP_024307590.1:p.Leu125=
NM_001256573.2:c.375G=	NP_001243502.1:p.Leu125=
NR_046317.2:n.1112G=
NM_000744.7:c.903G= MANE Select	NP_000735.1:p.Leu301=