Canonical Allele Identifier: CA511338717

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350400-C-G
• MyVariant Identifiers: chr20:g.61981752C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350400C>G , CM000682.2:g.63350400C>G	GRCh38
NC_000020.10:g.61981752C>G , CM000682.1:g.61981752C>G	GRCh37
NC_000020.9:g.61452196C>G	NCBI36
NG_011931.1:g.15944G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1011G>C MANE Select	ENSP00000359285.4:p.Thr337=
ENST00000370263.8:c.1011G>C	ENSP00000359285.4:p.Thr337=
ENST00000463705.5:n.1659G>C
ENST00000467563.3:n.1081G>C
ENST00000498043.6:c.1035G>C
ENST00000615287.4:c.798G>C	ENSP00000483388.1:p.Thr266=
ENST00000627000.1:c.*700G>C	ENSP00000486914.1:n.*700G>C
ENST00000630240.1:n.732G>C
NM_000744.6:c.1011G>C	NP_000735.1:p.Thr337=
NM_001256573.1:c.483G>C	NP_001243502.1:p.Thr161=
NR_046317.1:n.1267G>C
XM_011528524.1:c.798G>C	XP_011526826.1:p.Thr266=
XM_017027625.2:c.483G>C	XP_016883114.1:p.Thr161=
XM_024451822.1:c.483G>C	XP_024307590.1:p.Thr161=
NM_001256573.2:c.483G>C	NP_001243502.1:p.Thr161=
NR_046317.2:n.1220G>C
NM_000744.7:c.1011G>C MANE Select	NP_000735.1:p.Thr337=