Canonical Allele Identifier: CA2374743058

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350604G= , CM000682.2:g.63350604G=	GRCh38
NC_000020.10:g.61981956G= , CM000682.1:g.61981956G=	GRCh37
NC_000020.9:g.61452400G=	NCBI36
NG_011931.1:g.15740C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.807C= MANE Select	ENSP00000359285.4:p.Ser269=
ENST00000370263.8:c.807C=	ENSP00000359285.4:p.Ser269=
ENST00000463705.5:n.1455C=
ENST00000467563.3:n.877C=
ENST00000498043.6:c.831C=
ENST00000615287.4:c.594C=	ENSP00000483388.1:p.Ser198=
ENST00000627000.1:c.*496C=	ENSP00000486914.1:n.*496C=
ENST00000630240.1:n.528C=
NM_000744.6:c.807C=	NP_000735.1:p.Ser269=
NM_001256573.1:c.279C=	NP_001243502.1:p.Ser93=
NR_046317.1:n.1063C=
XM_011528524.1:c.594C=	XP_011526826.1:p.Ser198=
XM_017027625.2:c.279C=	XP_016883114.1:p.Ser93=
XM_024451822.1:c.279C=	XP_024307590.1:p.Ser93=
NM_001256573.2:c.279C=	NP_001243502.1:p.Ser93=
NR_046317.2:n.1016C=
NM_000744.7:c.807C= MANE Select	NP_000735.1:p.Ser269=