Canonical Allele Identifier: CA409635615

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350401-G-C
• MyVariant Identifiers: chr20:g.61981753G>C (hg19) ; chr20:g.63350401G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350401G>C , CM000682.2:g.63350401G>C	GRCh38
NC_000020.10:g.61981753G>C , CM000682.1:g.61981753G>C	GRCh37
NC_000020.9:g.61452197G>C	NCBI36
NG_011931.1:g.15943C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1010C>G MANE Select	ENSP00000359285.4:p.Thr337Arg
ENST00000370263.8:c.1010C>G	ENSP00000359285.4:p.Thr337Arg
ENST00000463705.5:n.1658C>G
ENST00000467563.3:n.1080C>G
ENST00000498043.6:c.1034C>G
ENST00000615287.4:c.797C>G	ENSP00000483388.1:p.Thr266Arg
ENST00000627000.1:c.*699C>G	ENSP00000486914.1:n.*699C>G
ENST00000630240.1:n.731C>G
NM_000744.6:c.1010C>G	NP_000735.1:p.Thr337Arg
NM_001256573.1:c.482C>G	NP_001243502.1:p.Thr161Arg
NR_046317.1:n.1266C>G
XM_011528524.1:c.797C>G	XP_011526826.1:p.Thr266Arg
XM_017027625.2:c.482C>G	XP_016883114.1:p.Thr161Arg
XM_024451822.1:c.482C>G	XP_024307590.1:p.Thr161Arg
NM_001256573.2:c.482C>G	NP_001243502.1:p.Thr161Arg
NR_046317.2:n.1219C>G
NM_000744.7:c.1010C>G MANE Select	NP_000735.1:p.Thr337Arg