Canonical Allele Identifier: CA2374743215

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350894G= , CM000682.2:g.63350894G=	GRCh38
NC_000020.10:g.61982246G= , CM000682.1:g.61982246G=	GRCh37
NC_000020.9:g.61452690G=	NCBI36
NG_011931.1:g.15450C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.517C= MANE Select	ENSP00000359285.4:p.Gln173=
ENST00000370263.8:c.517C=	ENSP00000359285.4:p.Gln173=
ENST00000463705.5:n.1165C=
ENST00000467563.3:n.587C=
ENST00000498043.6:c.541C=
ENST00000615287.4:c.304C=	ENSP00000483388.1:p.Gln102=
ENST00000627000.1:c.*206C=	ENSP00000486914.1:n.*206C=
ENST00000630240.1:n.238C=
NM_000744.6:c.517C=	NP_000735.1:p.Gln173=
NM_001256573.1:c.-12C=	NP_001243502.1:n.-12C=
NR_046317.1:n.773C=
XM_011528524.1:c.304C=	XP_011526826.1:p.Gln102=
XM_017027625.2:c.-12C=	XP_016883114.1:n.-12C=
XM_024451822.1:c.-12C=	XP_024307590.1:n.-12C=
NM_001256573.2:c.-12C=	NP_001243502.1:n.-12C=
NR_046317.2:n.726C=
NM_000744.7:c.517C= MANE Select	NP_000735.1:p.Gln173=