Canonical Allele Identifier: CA9957575

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349860C>T , CM000682.2:g.63349860C>T	GRCh38
NC_000020.10:g.61981212C>T , CM000682.1:g.61981212C>T	GRCh37
NC_000020.9:g.61451656C>T	NCBI36
NG_011931.1:g.16484G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1551G>A MANE Select	ENSP00000359285.4:p.Ser517=
ENST00000370263.8:c.1551G>A	ENSP00000359285.4:p.Ser517=
ENST00000463705.5:n.2199G>A
ENST00000467563.3:n.1621G>A
ENST00000498043.6:c.1575G>A
ENST00000615287.4:c.1338G>A	ENSP00000483388.1:p.Ser446=
ENST00000627000.1:c.*1240G>A	ENSP00000486914.1:n.*1240G>A
ENST00000630240.1:n.1272G>A
NM_000744.6:c.1551G>A	NP_000735.1:p.Ser517=
NM_001256573.1:c.1023G>A	NP_001243502.1:p.Ser341=
NR_046317.1:n.1807G>A
XM_011528524.1:c.1338G>A	XP_011526826.1:p.Ser446=
XM_017027625.2:c.1023G>A	XP_016883114.1:p.Ser341=
XM_024451822.1:c.1023G>A	XP_024307590.1:p.Ser341=
NM_001256573.2:c.1023G>A	NP_001243502.1:p.Ser341=
NR_046317.2:n.1760G>A
NM_000744.7:c.1551G>A MANE Select	NP_000735.1:p.Ser517=