Canonical Allele Identifier: CA409636843

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982002C>A (hg19) ; chr20:g.63350650C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350650C>A , CM000682.2:g.63350650C>A	GRCh38
NC_000020.10:g.61982002C>A , CM000682.1:g.61982002C>A	GRCh37
NC_000020.9:g.61452446C>A	NCBI36
NG_011931.1:g.15694G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.761G>T MANE Select	ENSP00000359285.4:p.Cys254Phe
ENST00000370263.8:c.761G>T	ENSP00000359285.4:p.Cys254Phe
ENST00000463705.5:n.1409G>T
ENST00000467563.3:n.831G>T
ENST00000498043.6:c.785G>T
ENST00000615287.4:c.548G>T	ENSP00000483388.1:p.Cys183Phe
ENST00000627000.1:c.*450G>T	ENSP00000486914.1:n.*450G>T
ENST00000630240.1:n.482G>T
NM_000744.6:c.761G>T	NP_000735.1:p.Cys254Phe
NM_001256573.1:c.233G>T	NP_001243502.1:p.Cys78Phe
NR_046317.1:n.1017G>T
XM_011528524.1:c.548G>T	XP_011526826.1:p.Cys183Phe
XM_017027625.2:c.233G>T	XP_016883114.1:p.Cys78Phe
XM_024451822.1:c.233G>T	XP_024307590.1:p.Cys78Phe
NM_001256573.2:c.233G>T	NP_001243502.1:p.Cys78Phe
NR_046317.2:n.970G>T
NM_000744.7:c.761G>T MANE Select	NP_000735.1:p.Cys254Phe