Canonical Allele Identifier: CA511339046

Gene: CHRNA4

Linked Data

• MyVariant Identifiers: chr20:g.61982268G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350916G>T , CM000682.2:g.63350916G>T	GRCh38
NC_000020.10:g.61982268G>T , CM000682.1:g.61982268G>T	GRCh37
NC_000020.9:g.61452712G>T	NCBI36
NG_011931.1:g.15428C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.495C>A MANE Select	ENSP00000359285.4:p.Val165=
ENST00000370263.8:c.495C>A	ENSP00000359285.4:p.Val165=
ENST00000463705.5:n.1143C>A
ENST00000467563.3:n.565C>A
ENST00000498043.6:c.519C>A
ENST00000615287.4:c.282C>A	ENSP00000483388.1:p.Val94=
ENST00000627000.1:c.*184C>A	ENSP00000486914.1:n.*184C>A
ENST00000628665.1:n.538C>A
ENST00000630240.1:n.216C>A
NM_000744.6:c.495C>A	NP_000735.1:p.Val165=
NM_001256573.1:c.-34C>A	NP_001243502.1:n.-34C>A
NR_046317.1:n.751C>A
XM_011528524.1:c.282C>A	XP_011526826.1:p.Val94=
XM_017027625.2:c.-34C>A	XP_016883114.1:n.-34C>A
XM_024451822.1:c.-34C>A	XP_024307590.1:n.-34C>A
NM_001256573.2:c.-34C>A	NP_001243502.1:n.-34C>A
NR_046317.2:n.704C>A
NM_000744.7:c.495C>A MANE Select	NP_000735.1:p.Val165=