Canonical Allele Identifier: CA511339135

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350760-G-A
• MyVariant Identifiers: chr20:g.61982112G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350760G>A , CM000682.2:g.63350760G>A	GRCh38
NC_000020.10:g.61982112G>A , CM000682.1:g.61982112G>A	GRCh37
NC_000020.9:g.61452556G>A	NCBI36
NG_011931.1:g.15584C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.651C>T MANE Select	ENSP00000359285.4:p.Thr217=
ENST00000370263.8:c.651C>T	ENSP00000359285.4:p.Thr217=
ENST00000463705.5:n.1299C>T
ENST00000467563.3:n.721C>T
ENST00000498043.6:c.675C>T
ENST00000615287.4:c.438C>T	ENSP00000483388.1:p.Thr146=
ENST00000627000.1:c.*340C>T	ENSP00000486914.1:n.*340C>T
ENST00000630240.1:n.372C>T
NM_000744.6:c.651C>T	NP_000735.1:p.Thr217=
NM_001256573.1:c.123C>T	NP_001243502.1:p.Thr41=
NR_046317.1:n.907C>T
XM_011528524.1:c.438C>T	XP_011526826.1:p.Thr146=
XM_017027625.2:c.123C>T	XP_016883114.1:p.Thr41=
XM_024451822.1:c.123C>T	XP_024307590.1:p.Thr41=
NM_001256573.2:c.123C>T	NP_001243502.1:p.Thr41=
NR_046317.2:n.860C>T
NM_000744.7:c.651C>T MANE Select	NP_000735.1:p.Thr217=