Canonical Allele Identifier: CA409636047

Gene: CHRNA4

Linked Data

• ClinVar Variation Id: 2108498
• ClinVar RCV Id: RCV003034209
• dbSNP Id: rs1264777378
• gnomAD v2: 20-61981821-C-T
• gnomAD v3: 20-63350469-C-T
• gnomAD v4: 20-63350469-C-T
• MyVariant Identifiers: chr20:g.61981821C>T (hg19) ; chr20:g.63350469C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350469C>T , CM000682.2:g.63350469C>T	GRCh38
NC_000020.10:g.61981821C>T , CM000682.1:g.61981821C>T	GRCh37
NC_000020.9:g.61452265C>T	NCBI36
NG_011931.1:g.15875G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.942G>A MANE Select	ENSP00000359285.4:p.Met314Ile
ENST00000370263.8:c.942G>A	ENSP00000359285.4:p.Met314Ile
ENST00000463705.5:n.1590G>A
ENST00000467563.3:n.1012G>A
ENST00000498043.6:c.966G>A
ENST00000615287.4:c.729G>A	ENSP00000483388.1:p.Met243Ile
ENST00000627000.1:c.*631G>A	ENSP00000486914.1:n.*631G>A
ENST00000630240.1:n.663G>A
NM_000744.6:c.942G>A	NP_000735.1:p.Met314Ile
NM_001256573.1:c.414G>A	NP_001243502.1:p.Met138Ile
NR_046317.1:n.1198G>A
XM_011528524.1:c.729G>A	XP_011526826.1:p.Met243Ile
XM_017027625.2:c.414G>A	XP_016883114.1:p.Met138Ile
XM_024451822.1:c.414G>A	XP_024307590.1:p.Met138Ile
NM_001256573.2:c.414G>A	NP_001243502.1:p.Met138Ile
NR_046317.2:n.1151G>A
NM_000744.7:c.942G>A MANE Select	NP_000735.1:p.Met314Ile