Canonical Allele Identifier: CA511338665

Gene: CHRNA4

Linked Data

• dbSNP Id: rs2123471620
• MyVariant Identifiers: chr20:g.61981704T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350352T>C , CM000682.2:g.63350352T>C	GRCh38
NC_000020.10:g.61981704T>C , CM000682.1:g.61981704T>C	GRCh37
NC_000020.9:g.61452148T>C	NCBI36
NG_011931.1:g.15992A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1059A>G MANE Select	ENSP00000359285.4:p.Pro353=
ENST00000370263.8:c.1059A>G	ENSP00000359285.4:p.Pro353=
ENST00000463705.5:n.1707A>G
ENST00000467563.3:n.1129A>G
ENST00000498043.6:c.1083A>G
ENST00000615287.4:c.846A>G	ENSP00000483388.1:p.Pro282=
ENST00000627000.1:c.*748A>G	ENSP00000486914.1:n.*748A>G
ENST00000630240.1:n.780A>G
NM_000744.6:c.1059A>G	NP_000735.1:p.Pro353=
NM_001256573.1:c.531A>G	NP_001243502.1:p.Pro177=
NR_046317.1:n.1315A>G
XM_011528524.1:c.846A>G	XP_011526826.1:p.Pro282=
XM_017027625.2:c.531A>G	XP_016883114.1:p.Pro177=
XM_024451822.1:c.531A>G	XP_024307590.1:p.Pro177=
NM_001256573.2:c.531A>G	NP_001243502.1:p.Pro177=
NR_046317.2:n.1268A>G
NM_000744.7:c.1059A>G MANE Select	NP_000735.1:p.Pro353=