Canonical Allele Identifier: CA409637504

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982140T>C (hg19) ; chr20:g.63350788T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350788T>C , CM000682.2:g.63350788T>C	GRCh38
NC_000020.10:g.61982140T>C , CM000682.1:g.61982140T>C	GRCh37
NC_000020.9:g.61452584T>C	NCBI36
NG_011931.1:g.15556A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.623A>G MANE Select	ENSP00000359285.4:p.Glu208Gly
ENST00000370263.8:c.623A>G	ENSP00000359285.4:p.Glu208Gly
ENST00000463705.5:n.1271A>G
ENST00000467563.3:n.693A>G
ENST00000498043.6:c.647A>G
ENST00000615287.4:c.410A>G	ENSP00000483388.1:p.Glu137Gly
ENST00000627000.1:c.*312A>G	ENSP00000486914.1:n.*312A>G
ENST00000630240.1:n.344A>G
NM_000744.6:c.623A>G	NP_000735.1:p.Glu208Gly
NM_001256573.1:c.95A>G	NP_001243502.1:p.Glu32Gly
NR_046317.1:n.879A>G
XM_011528524.1:c.410A>G	XP_011526826.1:p.Glu137Gly
XM_017027625.2:c.95A>G	XP_016883114.1:p.Glu32Gly
XM_024451822.1:c.95A>G	XP_024307590.1:p.Glu32Gly
NM_001256573.2:c.95A>G	NP_001243502.1:p.Glu32Gly
NR_046317.2:n.832A>G
NM_000744.7:c.623A>G MANE Select	NP_000735.1:p.Glu208Gly