Canonical Allele Identifier: CA409638134

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350884-G-A
• MyVariant Identifiers: chr20:g.61982236G>A (hg19) ; chr20:g.63350884G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350884G>A , CM000682.2:g.63350884G>A	GRCh38
NC_000020.10:g.61982236G>A , CM000682.1:g.61982236G>A	GRCh37
NC_000020.9:g.61452680G>A	NCBI36
NG_011931.1:g.15460C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.527C>T MANE Select	ENSP00000359285.4:p.Thr176Ile
ENST00000370263.8:c.527C>T	ENSP00000359285.4:p.Thr176Ile
ENST00000463705.5:n.1175C>T
ENST00000467563.3:n.597C>T
ENST00000498043.6:c.551C>T
ENST00000615287.4:c.314C>T	ENSP00000483388.1:p.Thr105Ile
ENST00000627000.1:c.*216C>T	ENSP00000486914.1:n.*216C>T
ENST00000630240.1:n.248C>T
NM_000744.6:c.527C>T	NP_000735.1:p.Thr176Ile
NM_001256573.1:c.-2C>T	NP_001243502.1:n.-2C>T
NR_046317.1:n.783C>T
XM_011528524.1:c.314C>T	XP_011526826.1:p.Thr105Ile
XM_017027625.2:c.-2C>T	XP_016883114.1:n.-2C>T
XM_024451822.1:c.-2C>T	XP_024307590.1:n.-2C>T
NM_001256573.2:c.-2C>T	NP_001243502.1:n.-2C>T
NR_046317.2:n.736C>T
NM_000744.7:c.527C>T MANE Select	NP_000735.1:p.Thr176Ile