Canonical Allele Identifier: CA317431487

Gene: CHRNA4

Linked Data

• dbSNP Id: rs201727307
• MyVariant Identifiers: chr20:g.61981017G>C (hg19) ; chr20:g.63349665G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349665G>C , CM000682.2:g.63349665G>C	GRCh38
NC_000020.10:g.61981017G>C , CM000682.1:g.61981017G>C	GRCh37
NC_000020.9:g.61451461G>C	NCBI36
NG_011931.1:g.16679C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.1746C>G MANE Select	ENSP00000359285.4:p.Asp582Glu
ENST00000370263.8:c.1746C>G	ENSP00000359285.4:p.Asp582Glu
ENST00000463705.5:n.2394C>G
ENST00000467563.3:n.1816C>G
ENST00000498043.6:c.1770C>G
ENST00000615287.4:c.1533C>G	ENSP00000483388.1:p.Asp511Glu
ENST00000627000.1:c.*1435C>G	ENSP00000486914.1:n.*1435C>G
ENST00000630240.1:n.1467C>G
NM_000744.6:c.1746C>G	NP_000735.1:p.Asp582Glu
NM_001256573.1:c.1218C>G	NP_001243502.1:p.Asp406Glu
NR_046317.1:n.2002C>G
XM_011528524.1:c.1533C>G	XP_011526826.1:p.Asp511Glu
XM_017027625.2:c.1218C>G	XP_016883114.1:p.Asp406Glu
XM_024451822.1:c.1218C>G	XP_024307590.1:p.Asp406Glu
NM_001256573.2:c.1218C>G	NP_001243502.1:p.Asp406Glu
NR_046317.2:n.1955C>G
NM_000744.7:c.1746C>G MANE Select	NP_000735.1:p.Asp582Glu