Canonical Allele Identifier: CA511338837

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61981917C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350565C>G , CM000682.2:g.63350565C>G	GRCh38
NC_000020.10:g.61981917C>G , CM000682.1:g.61981917C>G	GRCh37
NC_000020.9:g.61452361C>G	NCBI36
NG_011931.1:g.15779G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.846G>C MANE Select	ENSP00000359285.4:p.Leu282=
ENST00000370263.8:c.846G>C	ENSP00000359285.4:p.Leu282=
ENST00000463705.5:n.1494G>C
ENST00000467563.3:n.916G>C
ENST00000498043.6:c.870G>C
ENST00000615287.4:c.633G>C	ENSP00000483388.1:p.Leu211=
ENST00000627000.1:c.*535G>C	ENSP00000486914.1:n.*535G>C
ENST00000630240.1:n.567G>C
NM_000744.6:c.846G>C	NP_000735.1:p.Leu282=
NM_001256573.1:c.318G>C	NP_001243502.1:p.Leu106=
NR_046317.1:n.1102G>C
XM_011528524.1:c.633G>C	XP_011526826.1:p.Leu211=
XM_017027625.2:c.318G>C	XP_016883114.1:p.Leu106=
XM_024451822.1:c.318G>C	XP_024307590.1:p.Leu106=
NM_001256573.2:c.318G>C	NP_001243502.1:p.Leu106=
NR_046317.2:n.1055G>C
NM_000744.7:c.846G>C MANE Select	NP_000735.1:p.Leu282=