Canonical Allele Identifier: CA511338950

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981884G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350532G>C , CM000682.2:g.63350532G>C	GRCh38
NC_000020.10:g.61981884G>C , CM000682.1:g.61981884G>C	GRCh37
NC_000020.9:g.61452328G>C	NCBI36
NG_011931.1:g.15812C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.879C>G MANE Select	ENSP00000359285.4:p.Thr293=
ENST00000370263.8:c.879C>G	ENSP00000359285.4:p.Thr293=
ENST00000463705.5:n.1527C>G
ENST00000467563.3:n.949C>G
ENST00000498043.6:c.903C>G
ENST00000615287.4:c.666C>G	ENSP00000483388.1:p.Thr222=
ENST00000627000.1:c.*568C>G	ENSP00000486914.1:n.*568C>G
ENST00000630240.1:n.600C>G
NM_000744.6:c.879C>G	NP_000735.1:p.Thr293=
NM_001256573.1:c.351C>G	NP_001243502.1:p.Thr117=
NR_046317.1:n.1135C>G
XM_011528524.1:c.666C>G	XP_011526826.1:p.Thr222=
XM_017027625.2:c.351C>G	XP_016883114.1:p.Thr117=
XM_024451822.1:c.351C>G	XP_024307590.1:p.Thr117=
NM_001256573.2:c.351C>G	NP_001243502.1:p.Thr117=
NR_046317.2:n.1088C>G
NM_000744.7:c.879C>G MANE Select	NP_000735.1:p.Thr293=