Canonical Allele Identifier: CA511339014

Gene: CHRNA4

Linked Data

• COSMIC: COSM387261
• MyVariant Identifiers: chr20:g.61982235G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350883G>T , CM000682.2:g.63350883G>T	GRCh38
NC_000020.10:g.61982235G>T , CM000682.1:g.61982235G>T	GRCh37
NC_000020.9:g.61452679G>T	NCBI36
NG_011931.1:g.15461C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.528C>A MANE Select	ENSP00000359285.4:p.Thr176=
ENST00000370263.8:c.528C>A	ENSP00000359285.4:p.Thr176=
ENST00000463705.5:n.1176C>A
ENST00000467563.3:n.598C>A
ENST00000498043.6:c.552C>A
ENST00000615287.4:c.315C>A	ENSP00000483388.1:p.Thr105=
ENST00000627000.1:c.*217C>A	ENSP00000486914.1:n.*217C>A
ENST00000630240.1:n.249C>A
NM_000744.6:c.528C>A	NP_000735.1:p.Thr176=
NM_001256573.1:c.-1C>A	NP_001243502.1:n.-1C>A
NR_046317.1:n.784C>A
XM_011528524.1:c.315C>A	XP_011526826.1:p.Thr105=
XM_017027625.2:c.-1C>A	XP_016883114.1:n.-1C>A
XM_024451822.1:c.-1C>A	XP_024307590.1:n.-1C>A
NM_001256573.2:c.-1C>A	NP_001243502.1:n.-1C>A
NR_046317.2:n.737C>A
NM_000744.7:c.528C>A MANE Select	NP_000735.1:p.Thr176=