Canonical Allele Identifier: CA313583

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63349901C>T , CM000682.2:g.63349901C>T	GRCh38
NC_000020.10:g.61981253C>T , CM000682.1:g.61981253C>T	GRCh37
NC_000020.9:g.61451697C>T	NCBI36
NG_011931.1:g.16443G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.1510G>A MANE Select	ENSP00000359285.4:p.Gly504Ser
ENST00000370263.8:c.1510G>A	ENSP00000359285.4:p.Gly504Ser
ENST00000463705.5:n.2158G>A
ENST00000467563.3:n.1580G>A
ENST00000498043.6:c.1534G>A
ENST00000615287.4:c.1297G>A	ENSP00000483388.1:p.Gly433Ser
ENST00000627000.1:c.*1199G>A	ENSP00000486914.1:n.*1199G>A
ENST00000630240.1:n.1231G>A
NM_000744.6:c.1510G>A	NP_000735.1:p.Gly504Ser
NM_001256573.1:c.982G>A	NP_001243502.1:p.Gly328Ser
NR_046317.1:n.1766G>A
XM_011528524.1:c.1297G>A	XP_011526826.1:p.Gly433Ser
XM_017027625.2:c.982G>A	XP_016883114.1:p.Gly328Ser
XM_024451822.1:c.982G>A	XP_024307590.1:p.Gly328Ser
NM_001256573.2:c.982G>A	NP_001243502.1:p.Gly328Ser
NR_046317.2:n.1719G>A
NM_000744.7:c.1510G>A MANE Select	NP_000735.1:p.Gly504Ser