Canonical Allele Identifier: CA2374743072

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350623_63350628delinsAGCACG , CM000682.2:g.63350623_63350628delinsAGCACG	GRCh38
NC_000020.10:g.61981975_61981980delinsAGCACG , CM000682.1:g.61981975_61981980delinsAGCACG	GRCh37
NC_000020.9:g.61452419_61452424delinsAGCACG	NCBI36
NG_011931.1:g.15716_15721delinsCGTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.783_788delinsCGTGCT MANE Select	ENSP00000359285.4:p.Thr261=
ENST00000370263.8:c.783_788delinsCGTGCT	ENSP00000359285.4:p.Thr261=
ENST00000463705.5:n.1431_1436delinsCGTGCT
ENST00000467563.3:n.853_858delinsCGTGCT
ENST00000498043.6:c.807_812delinsCGTGCT
ENST00000615287.4:c.570_575delinsCGTGCT	ENSP00000483388.1:p.Thr190=
ENST00000627000.1:c.*472_*477delinsCGTGCT	ENSP00000486914.1:n.*472_*477delinsCGTGCT
ENST00000630240.1:n.504_509delinsCGTGCT
NM_000744.6:c.783_788delinsCGTGCT	NP_000735.1:p.Thr261=
NM_001256573.1:c.255_260delinsCGTGCT	NP_001243502.1:p.Thr85=
NR_046317.1:n.1039_1044delinsCGTGCT
XM_011528524.1:c.570_575delinsCGTGCT	XP_011526826.1:p.Thr190=
XM_017027625.2:c.255_260delinsCGTGCT	XP_016883114.1:p.Thr85=
XM_024451822.1:c.255_260delinsCGTGCT	XP_024307590.1:p.Thr85=
NM_001256573.2:c.255_260delinsCGTGCT	NP_001243502.1:p.Thr85=
NR_046317.2:n.992_997delinsCGTGCT
NM_000744.7:c.783_788delinsCGTGCT MANE Select	NP_000735.1:p.Thr261=