Canonical Allele Identifier: CA409638045

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982218C>T (hg19) ; chr20:g.63350866C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350866C>T , CM000682.2:g.63350866C>T	GRCh38
NC_000020.10:g.61982218C>T , CM000682.1:g.61982218C>T	GRCh37
NC_000020.9:g.61452662C>T	NCBI36
NG_011931.1:g.15478G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.545G>A MANE Select	ENSP00000359285.4:p.Trp182Ter
ENST00000370263.8:c.545G>A	ENSP00000359285.4:p.Trp182Ter
ENST00000463705.5:n.1193G>A
ENST00000467563.3:n.615G>A
ENST00000498043.6:c.569G>A
ENST00000615287.4:c.332G>A	ENSP00000483388.1:p.Trp111Ter
ENST00000627000.1:c.*234G>A	ENSP00000486914.1:n.*234G>A
ENST00000630240.1:n.266G>A
NM_000744.6:c.545G>A	NP_000735.1:p.Trp182Ter
NM_001256573.1:c.17G>A	NP_001243502.1:p.Trp6Ter
NR_046317.1:n.801G>A
XM_011528524.1:c.332G>A	XP_011526826.1:p.Trp111Ter
XM_017027625.2:c.17G>A	XP_016883114.1:p.Trp6Ter
XM_024451822.1:c.17G>A	XP_024307590.1:p.Trp6Ter
NM_001256573.2:c.17G>A	NP_001243502.1:p.Trp6Ter
NR_046317.2:n.754G>A
NM_000744.7:c.545G>A MANE Select	NP_000735.1:p.Trp182Ter