Canonical Allele Identifier: CA2577452935

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350482_63350483insT , CM000682.2:g.63350482_63350483insT	GRCh38
NC_000020.10:g.61981834_61981835insT , CM000682.1:g.61981834_61981835insT	GRCh37
NC_000020.9:g.61452278_61452279insT	NCBI36
NG_011931.1:g.15861_15862insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.928_929insA MANE Select	ENSP00000359285.4:p.Leu310HisfsTer?
ENST00000370263.8:c.928_929insA	ENSP00000359285.4:p.Leu310HisfsTer?
ENST00000463705.5:n.1576_1577insA
ENST00000467563.3:n.998_999insA
ENST00000498043.6:c.952_953insA
ENST00000615287.4:c.715_716insA	ENSP00000483388.1:p.Leu239HisfsTer?
ENST00000627000.1:c.*617_*618insA	ENSP00000486914.1:n.*617_*618insA
ENST00000630240.1:n.649_650insA
NM_000744.6:c.928_929insA	NP_000735.1:p.Leu310HisfsTer?
NM_001256573.1:c.400_401insA	NP_001243502.1:p.Leu134HisfsTer?
NR_046317.1:n.1184_1185insA
XM_011528524.1:c.715_716insA	XP_011526826.1:p.Leu239HisfsTer?
XM_017027625.2:c.400_401insA	XP_016883114.1:p.Leu134HisfsTer?
XM_024451822.1:c.400_401insA	XP_024307590.1:p.Leu134HisfsTer?
NM_001256573.2:c.400_401insA	NP_001243502.1:p.Leu134HisfsTer?
NR_046317.2:n.1137_1138insA
NM_000744.7:c.928_929insA MANE Select	NP_000735.1:p.Leu310HisfsTer?