Canonical Allele Identifier: CA409636429

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981895G>T (hg19) ; chr20:g.63350543G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350543G>T , CM000682.2:g.63350543G>T	GRCh38
NC_000020.10:g.61981895G>T , CM000682.1:g.61981895G>T	GRCh37
NC_000020.9:g.61452339G>T	NCBI36
NG_011931.1:g.15801C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.868C>A MANE Select	ENSP00000359285.4:p.Leu290Met
ENST00000370263.8:c.868C>A	ENSP00000359285.4:p.Leu290Met
ENST00000463705.5:n.1516C>A
ENST00000467563.3:n.938C>A
ENST00000498043.6:c.892C>A
ENST00000615287.4:c.655C>A	ENSP00000483388.1:p.Leu219Met
ENST00000627000.1:c.*557C>A	ENSP00000486914.1:n.*557C>A
ENST00000630240.1:n.589C>A
NM_000744.6:c.868C>A	NP_000735.1:p.Leu290Met
NM_001256573.1:c.340C>A	NP_001243502.1:p.Leu114Met
NR_046317.1:n.1124C>A
XM_011528524.1:c.655C>A	XP_011526826.1:p.Leu219Met
XM_017027625.2:c.340C>A	XP_016883114.1:p.Leu114Met
XM_024451822.1:c.340C>A	XP_024307590.1:p.Leu114Met
NM_001256573.2:c.340C>A	NP_001243502.1:p.Leu114Met
NR_046317.2:n.1077C>A
NM_000744.7:c.868C>A MANE Select	NP_000735.1:p.Leu290Met