Canonical Allele Identifier: CA409636561

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981931A>G (hg19) ; chr20:g.63350579A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350579A>G , CM000682.2:g.63350579A>G	GRCh38
NC_000020.10:g.61981931A>G , CM000682.1:g.61981931A>G	GRCh37
NC_000020.9:g.61452375A>G	NCBI36
NG_011931.1:g.15765T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.832T>C MANE Select	ENSP00000359285.4:p.Cys278Arg
ENST00000370263.8:c.832T>C	ENSP00000359285.4:p.Cys278Arg
ENST00000463705.5:n.1480T>C
ENST00000467563.3:n.902T>C
ENST00000498043.6:c.856T>C
ENST00000615287.4:c.619T>C	ENSP00000483388.1:p.Cys207Arg
ENST00000627000.1:c.*521T>C	ENSP00000486914.1:n.*521T>C
ENST00000630240.1:n.553T>C
NM_000744.6:c.832T>C	NP_000735.1:p.Cys278Arg
NM_001256573.1:c.304T>C	NP_001243502.1:p.Cys102Arg
NR_046317.1:n.1088T>C
XM_011528524.1:c.619T>C	XP_011526826.1:p.Cys207Arg
XM_017027625.2:c.304T>C	XP_016883114.1:p.Cys102Arg
XM_024451822.1:c.304T>C	XP_024307590.1:p.Cys102Arg
NM_001256573.2:c.304T>C	NP_001243502.1:p.Cys102Arg
NR_046317.2:n.1041T>C
NM_000744.7:c.832T>C MANE Select	NP_000735.1:p.Cys278Arg