Canonical Allele Identifier: CA2374743226

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350909A= , CM000682.2:g.63350909A=	GRCh38
NC_000020.10:g.61982261A= , CM000682.1:g.61982261A=	GRCh37
NC_000020.9:g.61452705A=	NCBI36
NG_011931.1:g.15435T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.502T= MANE Select	ENSP00000359285.4:p.Phe168=
ENST00000370263.8:c.502T=	ENSP00000359285.4:p.Phe168=
ENST00000463705.5:n.1150T=
ENST00000467563.3:n.572T=
ENST00000498043.6:c.526T=
ENST00000615287.4:c.289T=	ENSP00000483388.1:p.Phe97=
ENST00000627000.1:c.*191T=	ENSP00000486914.1:n.*191T=
ENST00000628665.1:n.545T=
ENST00000630240.1:n.223T=
NM_000744.6:c.502T=	NP_000735.1:p.Phe168=
NM_001256573.1:c.-27T=	NP_001243502.1:n.-27T=
NR_046317.1:n.758T=
XM_011528524.1:c.289T=	XP_011526826.1:p.Phe97=
XM_017027625.2:c.-27T=	XP_016883114.1:n.-27T=
XM_024451822.1:c.-27T=	XP_024307590.1:n.-27T=
NM_001256573.2:c.-27T=	NP_001243502.1:n.-27T=
NR_046317.2:n.711T=
NM_000744.7:c.502T= MANE Select	NP_000735.1:p.Phe168=