Canonical Allele Identifier: CA2374742945

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350398T= , CM000682.2:g.63350398T=	GRCh38
NC_000020.10:g.61981750T= , CM000682.1:g.61981750T=	GRCh37
NC_000020.9:g.61452194T=	NCBI36
NG_011931.1:g.15946A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1013A= MANE Select	ENSP00000359285.4:p.His338=
ENST00000370263.8:c.1013A=	ENSP00000359285.4:p.His338=
ENST00000463705.5:n.1661A=
ENST00000467563.3:n.1083A=
ENST00000498043.6:c.1037A=
ENST00000615287.4:c.800A=	ENSP00000483388.1:p.His267=
ENST00000627000.1:c.*702A=	ENSP00000486914.1:n.*702A=
ENST00000630240.1:n.734A=
NM_000744.6:c.1013A=	NP_000735.1:p.His338=
NM_001256573.1:c.485A=	NP_001243502.1:p.His162=
NR_046317.1:n.1269A=
XM_011528524.1:c.800A=	XP_011526826.1:p.His267=
XM_017027625.2:c.485A=	XP_016883114.1:p.His162=
XM_024451822.1:c.485A=	XP_024307590.1:p.His162=
NM_001256573.2:c.485A=	NP_001243502.1:p.His162=
NR_046317.2:n.1222A=
NM_000744.7:c.1013A= MANE Select	NP_000735.1:p.His338=