Canonical Allele Identifier: CA409638263

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982254A>C (hg19) ; chr20:g.63350902A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350902A>C , CM000682.2:g.63350902A>C	GRCh38
NC_000020.10:g.61982254A>C , CM000682.1:g.61982254A>C	GRCh37
NC_000020.9:g.61452698A>C	NCBI36
NG_011931.1:g.15442T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.509T>G MANE Select	ENSP00000359285.4:p.Phe170Cys
ENST00000370263.8:c.509T>G	ENSP00000359285.4:p.Phe170Cys
ENST00000463705.5:n.1157T>G
ENST00000467563.3:n.579T>G
ENST00000498043.6:c.533T>G
ENST00000615287.4:c.296T>G	ENSP00000483388.1:p.Phe99Cys
ENST00000627000.1:c.*198T>G	ENSP00000486914.1:n.*198T>G
ENST00000630240.1:n.230T>G
NM_000744.6:c.509T>G	NP_000735.1:p.Phe170Cys
NM_001256573.1:c.-20T>G	NP_001243502.1:n.-20T>G
NR_046317.1:n.765T>G
XM_011528524.1:c.296T>G	XP_011526826.1:p.Phe99Cys
XM_017027625.2:c.-20T>G	XP_016883114.1:n.-20T>G
XM_024451822.1:c.-20T>G	XP_024307590.1:n.-20T>G
NM_001256573.2:c.-20T>G	NP_001243502.1:n.-20T>G
NR_046317.2:n.718T>G
NM_000744.7:c.509T>G MANE Select	NP_000735.1:p.Phe170Cys