Canonical Allele Identifier: CA409632793

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981172A>C (hg19) ; chr20:g.63349820A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349820A>C , CM000682.2:g.63349820A>C	GRCh38
NC_000020.10:g.61981172A>C , CM000682.1:g.61981172A>C	GRCh37
NC_000020.9:g.61451616A>C	NCBI36
NG_011931.1:g.16524T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1591T>G MANE Select	ENSP00000359285.4:p.Cys531Gly
ENST00000370263.8:c.1591T>G	ENSP00000359285.4:p.Cys531Gly
ENST00000463705.5:n.2239T>G
ENST00000467563.3:n.1661T>G
ENST00000498043.6:c.1615T>G
ENST00000615287.4:c.1378T>G	ENSP00000483388.1:p.Cys460Gly
ENST00000627000.1:c.*1280T>G	ENSP00000486914.1:n.*1280T>G
ENST00000630240.1:n.1312T>G
NM_000744.6:c.1591T>G	NP_000735.1:p.Cys531Gly
NM_001256573.1:c.1063T>G	NP_001243502.1:p.Cys355Gly
NR_046317.1:n.1847T>G
XM_011528524.1:c.1378T>G	XP_011526826.1:p.Cys460Gly
XM_017027625.2:c.1063T>G	XP_016883114.1:p.Cys355Gly
XM_024451822.1:c.1063T>G	XP_024307590.1:p.Cys355Gly
NM_001256573.2:c.1063T>G	NP_001243502.1:p.Cys355Gly
NR_046317.2:n.1800T>G
NM_000744.7:c.1591T>G MANE Select	NP_000735.1:p.Cys531Gly