Canonical Allele Identifier: CA409635295

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981691T>C (hg19) ; chr20:g.63350339T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350339T>C , CM000682.2:g.63350339T>C	GRCh38
NC_000020.10:g.61981691T>C , CM000682.1:g.61981691T>C	GRCh37
NC_000020.9:g.61452135T>C	NCBI36
NG_011931.1:g.16005A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1072A>G MANE Select	ENSP00000359285.4:p.Met358Val
ENST00000370263.8:c.1072A>G	ENSP00000359285.4:p.Met358Val
ENST00000463705.5:n.1720A>G
ENST00000467563.3:n.1142A>G
ENST00000498043.6:c.1096A>G
ENST00000615287.4:c.859A>G	ENSP00000483388.1:p.Met287Val
ENST00000627000.1:c.*761A>G	ENSP00000486914.1:n.*761A>G
ENST00000630240.1:n.793A>G
NM_000744.6:c.1072A>G	NP_000735.1:p.Met358Val
NM_001256573.1:c.544A>G	NP_001243502.1:p.Met182Val
NR_046317.1:n.1328A>G
XM_011528524.1:c.859A>G	XP_011526826.1:p.Met287Val
XM_017027625.2:c.544A>G	XP_016883114.1:p.Met182Val
XM_024451822.1:c.544A>G	XP_024307590.1:p.Met182Val
NM_001256573.2:c.544A>G	NP_001243502.1:p.Met182Val
NR_046317.2:n.1281A>G
NM_000744.7:c.1072A>G MANE Select	NP_000735.1:p.Met358Val