Canonical Allele Identifier: CA2374742959

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350424_63350425delinsGT , CM000682.2:g.63350424_63350425delinsGT	GRCh38
NC_000020.10:g.61981776_61981777delinsGT , CM000682.1:g.61981776_61981777delinsGT	GRCh37
NC_000020.9:g.61452220_61452221delinsGT	NCBI36
NG_011931.1:g.15919_15920delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.986_987delinsAC MANE Select	ENSP00000359285.4:p.Asn329=
ENST00000370263.8:c.986_987delinsAC	ENSP00000359285.4:p.Asn329=
ENST00000463705.5:n.1634_1635delinsAC
ENST00000467563.3:n.1056_1057delinsAC
ENST00000498043.6:c.1010_1011delinsAC
ENST00000615287.4:c.773_774delinsAC	ENSP00000483388.1:p.Asn258=
ENST00000627000.1:c.*675_*676delinsAC	ENSP00000486914.1:n.*675_*676delinsAC
ENST00000630240.1:n.707_708delinsAC
NM_000744.6:c.986_987delinsAC	NP_000735.1:p.Asn329=
NM_001256573.1:c.458_459delinsAC	NP_001243502.1:p.Asn153=
NR_046317.1:n.1242_1243delinsAC
XM_011528524.1:c.773_774delinsAC	XP_011526826.1:p.Asn258=
XM_017027625.2:c.458_459delinsAC	XP_016883114.1:p.Asn153=
XM_024451822.1:c.458_459delinsAC	XP_024307590.1:p.Asn153=
NM_001256573.2:c.458_459delinsAC	NP_001243502.1:p.Asn153=
NR_046317.2:n.1195_1196delinsAC
NM_000744.7:c.986_987delinsAC MANE Select	NP_000735.1:p.Asn329=