Canonical Allele Identifier: CA409636803

Gene: CHRNA4

Linked Data

• ClinVar Variation Id: 2788449
• ClinVar RCV Id: RCV003746781
• gnomAD v4: 20-63350640-G-C
• MyVariant Identifiers: chr20:g.61981992G>C (hg19) ; chr20:g.63350640G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350640G>C , CM000682.2:g.63350640G>C	GRCh38
NC_000020.10:g.61981992G>C , CM000682.1:g.61981992G>C	GRCh37
NC_000020.9:g.61452436G>C	NCBI36
NG_011931.1:g.15704C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.771C>G MANE Select	ENSP00000359285.4:p.Ile257Met
ENST00000370263.8:c.771C>G	ENSP00000359285.4:p.Ile257Met
ENST00000463705.5:n.1419C>G
ENST00000467563.3:n.841C>G
ENST00000498043.6:c.795C>G
ENST00000615287.4:c.558C>G	ENSP00000483388.1:p.Ile186Met
ENST00000627000.1:c.*460C>G	ENSP00000486914.1:n.*460C>G
ENST00000630240.1:n.492C>G
NM_000744.6:c.771C>G	NP_000735.1:p.Ile257Met
NM_001256573.1:c.243C>G	NP_001243502.1:p.Ile81Met
NR_046317.1:n.1027C>G
XM_011528524.1:c.558C>G	XP_011526826.1:p.Ile186Met
XM_017027625.2:c.243C>G	XP_016883114.1:p.Ile81Met
XM_024451822.1:c.243C>G	XP_024307590.1:p.Ile81Met
NM_001256573.2:c.243C>G	NP_001243502.1:p.Ile81Met
NR_046317.2:n.980C>G
NM_000744.7:c.771C>G MANE Select	NP_000735.1:p.Ile257Met