Canonical Allele Identifier: CA409637217

Gene: CHRNA4

Linked Data

• gnomAD v4: 20-63350739-C-G
• MyVariant Identifiers: chr20:g.61982091C>G (hg19) ; chr20:g.63350739C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350739C>G , CM000682.2:g.63350739C>G	GRCh38
NC_000020.10:g.61982091C>G , CM000682.1:g.61982091C>G	GRCh37
NC_000020.9:g.61452535C>G	NCBI36
NG_011931.1:g.15605G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000370263.9:c.672G>C MANE Select	ENSP00000359285.4:p.Glu224Asp
ENST00000370263.8:c.672G>C	ENSP00000359285.4:p.Glu224Asp
ENST00000463705.5:n.1320G>C
ENST00000467563.3:n.742G>C
ENST00000498043.6:c.696G>C
ENST00000615287.4:c.459G>C	ENSP00000483388.1:p.Glu153Asp
ENST00000627000.1:c.*361G>C	ENSP00000486914.1:n.*361G>C
ENST00000630240.1:n.393G>C
NM_000744.6:c.672G>C	NP_000735.1:p.Glu224Asp
NM_001256573.1:c.144G>C	NP_001243502.1:p.Glu48Asp
NR_046317.1:n.928G>C
XM_011528524.1:c.459G>C	XP_011526826.1:p.Glu153Asp
XM_017027625.2:c.144G>C	XP_016883114.1:p.Glu48Asp
XM_024451822.1:c.144G>C	XP_024307590.1:p.Glu48Asp
NM_001256573.2:c.144G>C	NP_001243502.1:p.Glu48Asp
NR_046317.2:n.881G>C
NM_000744.7:c.672G>C MANE Select	NP_000735.1:p.Glu224Asp