Canonical Allele Identifier: CA511339022

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350892-C-T
• MyVariant Identifiers: chr20:g.61982244C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350892C>T , CM000682.2:g.63350892C>T	GRCh38
NC_000020.10:g.61982244C>T , CM000682.1:g.61982244C>T	GRCh37
NC_000020.9:g.61452688C>T	NCBI36
NG_011931.1:g.15452G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.519G>A MANE Select	ENSP00000359285.4:p.Gln173=
ENST00000370263.8:c.519G>A	ENSP00000359285.4:p.Gln173=
ENST00000463705.5:n.1167G>A
ENST00000467563.3:n.589G>A
ENST00000498043.6:c.543G>A
ENST00000615287.4:c.306G>A	ENSP00000483388.1:p.Gln102=
ENST00000627000.1:c.*208G>A	ENSP00000486914.1:n.*208G>A
ENST00000630240.1:n.240G>A
NM_000744.6:c.519G>A	NP_000735.1:p.Gln173=
NM_001256573.1:c.-10G>A	NP_001243502.1:n.-10G>A
NR_046317.1:n.775G>A
XM_011528524.1:c.306G>A	XP_011526826.1:p.Gln102=
XM_017027625.2:c.-10G>A	XP_016883114.1:n.-10G>A
XM_024451822.1:c.-10G>A	XP_024307590.1:n.-10G>A
NM_001256573.2:c.-10G>A	NP_001243502.1:n.-10G>A
NR_046317.2:n.728G>A
NM_000744.7:c.519G>A MANE Select	NP_000735.1:p.Gln173=