Canonical Allele Identifier: CA2374743223

Gene: CHRNA4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63350903_63350904delinsAG , CM000682.2:g.63350903_63350904delinsAG	GRCh38
NC_000020.10:g.61982255_61982256delinsAG , CM000682.1:g.61982255_61982256delinsAG	GRCh37
NC_000020.9:g.61452699_61452700delinsAG	NCBI36
NG_011931.1:g.15440_15441delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370263.9:c.507_508delinsCT MANE Select	ENSP00000359285.4:p.Pro169=
ENST00000370263.8:c.507_508delinsCT	ENSP00000359285.4:p.Pro169=
ENST00000463705.5:n.1155_1156delinsCT
ENST00000467563.3:n.577_578delinsCT
ENST00000498043.6:c.531_532delinsCT
ENST00000615287.4:c.294_295delinsCT	ENSP00000483388.1:p.Pro98=
ENST00000627000.1:c.*196_*197delinsCT	ENSP00000486914.1:n.*196_*197delinsCT
ENST00000630240.1:n.228_229delinsCT
NM_000744.6:c.507_508delinsCT	NP_000735.1:p.Pro169=
NM_001256573.1:c.-22_-21delinsCT	NP_001243502.1:n.-22_-21delinsCT
NR_046317.1:n.763_764delinsCT
XM_011528524.1:c.294_295delinsCT	XP_011526826.1:p.Pro98=
XM_017027625.2:c.-22_-21delinsCT	XP_016883114.1:n.-22_-21delinsCT
XM_024451822.1:c.-22_-21delinsCT	XP_024307590.1:n.-22_-21delinsCT
NM_001256573.2:c.-22_-21delinsCT	NP_001243502.1:n.-22_-21delinsCT
NR_046317.2:n.716_717delinsCT
NM_000744.7:c.507_508delinsCT MANE Select	NP_000735.1:p.Pro169=