Canonical Allele Identifier: CA511338951

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982196G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350844G>T , CM000682.2:g.63350844G>T	GRCh38
NC_000020.10:g.61982196G>T , CM000682.1:g.61982196G>T	GRCh37
NC_000020.9:g.61452640G>T	NCBI36
NG_011931.1:g.15500C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.567C>A MANE Select	ENSP00000359285.4:p.Ile189=
ENST00000370263.8:c.567C>A	ENSP00000359285.4:p.Ile189=
ENST00000463705.5:n.1215C>A
ENST00000467563.3:n.637C>A
ENST00000498043.6:c.591C>A
ENST00000615287.4:c.354C>A	ENSP00000483388.1:p.Ile118=
ENST00000627000.1:c.*256C>A	ENSP00000486914.1:n.*256C>A
ENST00000630240.1:n.288C>A
NM_000744.6:c.567C>A	NP_000735.1:p.Ile189=
NM_001256573.1:c.39C>A	NP_001243502.1:p.Ile13=
NR_046317.1:n.823C>A
XM_011528524.1:c.354C>A	XP_011526826.1:p.Ile118=
XM_017027625.2:c.39C>A	XP_016883114.1:p.Ile13=
XM_024451822.1:c.39C>A	XP_024307590.1:p.Ile13=
NM_001256573.2:c.39C>A	NP_001243502.1:p.Ile13=
NR_046317.2:n.776C>A
NM_000744.7:c.567C>A MANE Select	NP_000735.1:p.Ile189=