Canonical Allele Identifier: CA245965

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349957C>T , CM000682.2:g.63349957C>T	GRCh38
NC_000020.10:g.61981309C>T , CM000682.1:g.61981309C>T	GRCh37
NC_000020.9:g.61451753C>T	NCBI36
NG_011931.1:g.16387G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1454G>A MANE Select	ENSP00000359285.4:p.Arg485Gln
ENST00000370263.8:c.1454G>A	ENSP00000359285.4:p.Arg485Gln
ENST00000463705.5:n.2102G>A
ENST00000467563.3:n.1524G>A
ENST00000498043.6:c.1478G>A
ENST00000615287.4:c.1241G>A	ENSP00000483388.1:p.Arg414Gln
ENST00000627000.1:c.*1143G>A	ENSP00000486914.1:n.*1143G>A
ENST00000630240.1:n.1175G>A
NM_000744.6:c.1454G>A	NP_000735.1:p.Arg485Gln
NM_001256573.1:c.926G>A	NP_001243502.1:p.Arg309Gln
NR_046317.1:n.1710G>A
XM_011528524.1:c.1241G>A	XP_011526826.1:p.Arg414Gln
XM_017027625.2:c.926G>A	XP_016883114.1:p.Arg309Gln
XM_024451822.1:c.926G>A	XP_024307590.1:p.Arg309Gln
NM_001256573.2:c.926G>A	NP_001243502.1:p.Arg309Gln
NR_046317.2:n.1663G>A
NM_000744.7:c.1454G>A MANE Select	NP_000735.1:p.Arg485Gln