Canonical Allele Identifier: CA9957556

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349744G>C , CM000682.2:g.63349744G>C	GRCh38
NC_000020.10:g.61981096G>C , CM000682.1:g.61981096G>C	GRCh37
NC_000020.9:g.61451540G>C	NCBI36
NG_011931.1:g.16600C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1667C>G MANE Select	ENSP00000359285.4:p.Pro556Arg
ENST00000370263.8:c.1667C>G	ENSP00000359285.4:p.Pro556Arg
ENST00000463705.5:n.2315C>G
ENST00000467563.3:n.1737C>G
ENST00000498043.6:c.1691C>G
ENST00000615287.4:c.1454C>G	ENSP00000483388.1:p.Pro485Arg
ENST00000627000.1:c.*1356C>G	ENSP00000486914.1:n.*1356C>G
ENST00000630240.1:n.1388C>G
NM_000744.6:c.1667C>G	NP_000735.1:p.Pro556Arg
NM_001256573.1:c.1139C>G	NP_001243502.1:p.Pro380Arg
NR_046317.1:n.1923C>G
XM_011528524.1:c.1454C>G	XP_011526826.1:p.Pro485Arg
XM_017027625.2:c.1139C>G	XP_016883114.1:p.Pro380Arg
XM_024451822.1:c.1139C>G	XP_024307590.1:p.Pro380Arg
NM_001256573.2:c.1139C>G	NP_001243502.1:p.Pro380Arg
NR_046317.2:n.1876C>G
NM_000744.7:c.1667C>G MANE Select	NP_000735.1:p.Pro556Arg