Canonical Allele Identifier: CA409636492

Gene: CHRNA4

Linked Data

• ClinVar Variation Id: 969721
• ClinVar RCV Id: RCV001245132
• dbSNP Id: rs28931591
• MyVariant Identifiers: chr20:g.61981912G>C (hg19) ; chr20:g.63350560G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350560G>C , CM000682.2:g.63350560G>C	GRCh38
NC_000020.10:g.61981912G>C , CM000682.1:g.61981912G>C	GRCh37
NC_000020.9:g.61452356G>C	NCBI36
NG_011931.1:g.15784C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.851C>G MANE Select	ENSP00000359285.4:p.Ser284Trp
ENST00000370263.8:c.851C>G	ENSP00000359285.4:p.Ser284Trp
ENST00000463705.5:n.1499C>G
ENST00000467563.3:n.921C>G
ENST00000498043.6:c.875C>G
ENST00000615287.4:c.638C>G	ENSP00000483388.1:p.Ser213Trp
ENST00000627000.1:c.*540C>G	ENSP00000486914.1:n.*540C>G
ENST00000630240.1:n.572C>G
NM_000744.6:c.851C>G	NP_000735.1:p.Ser284Trp
NM_001256573.1:c.323C>G	NP_001243502.1:p.Ser108Trp
NR_046317.1:n.1107C>G
XM_011528524.1:c.638C>G	XP_011526826.1:p.Ser213Trp
XM_017027625.2:c.323C>G	XP_016883114.1:p.Ser108Trp
XM_024451822.1:c.323C>G	XP_024307590.1:p.Ser108Trp
NM_001256573.2:c.323C>G	NP_001243502.1:p.Ser108Trp
NR_046317.2:n.1060C>G
NM_000744.7:c.851C>G MANE Select	NP_000735.1:p.Ser284Trp