Canonical Allele Identifier: CA9957721

Gene: CHRNA4

Linked Data

• ClinVar Variation Id: 1005320
• ClinVar RCV Id: RCV001302173
• dbSNP Id: rs758885593
• ExAC: 20:61981946 C / T
• gnomAD v2: 20-61981946-C-T
• gnomAD v3: 20-63350594-C-T
• gnomAD v4: 20-63350594-C-T
• MyVariant Identifiers: chr20:g.61981946C>T (hg19) ; chr20:g.63350594C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350594C>T , CM000682.2:g.63350594C>T	GRCh38
NC_000020.10:g.61981946C>T , CM000682.1:g.61981946C>T	GRCh37
NC_000020.9:g.61452390C>T	NCBI36
NG_011931.1:g.15750G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.817G>A MANE Select	ENSP00000359285.4:p.Glu273Lys
ENST00000370263.8:c.817G>A	ENSP00000359285.4:p.Glu273Lys
ENST00000463705.5:n.1465G>A
ENST00000467563.3:n.887G>A
ENST00000498043.6:c.841G>A
ENST00000615287.4:c.604G>A	ENSP00000483388.1:p.Glu202Lys
ENST00000627000.1:c.*506G>A	ENSP00000486914.1:n.*506G>A
ENST00000630240.1:n.538G>A
NM_000744.6:c.817G>A	NP_000735.1:p.Glu273Lys
NM_001256573.1:c.289G>A	NP_001243502.1:p.Glu97Lys
NR_046317.1:n.1073G>A
XM_011528524.1:c.604G>A	XP_011526826.1:p.Glu202Lys
XM_017027625.2:c.289G>A	XP_016883114.1:p.Glu97Lys
XM_024451822.1:c.289G>A	XP_024307590.1:p.Glu97Lys
NM_001256573.2:c.289G>A	NP_001243502.1:p.Glu97Lys
NR_046317.2:n.1026G>A
NM_000744.7:c.817G>A MANE Select	NP_000735.1:p.Glu273Lys