Canonical Allele Identifier: CA2189589992

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601861_78601863delinsGCA , CM000677.2:g.78601861_78601863delinsGCA	GRCh38
NC_000015.9:g.78894203_78894205delinsGCA , CM000677.1:g.78894203_78894205delinsGCA	GRCh37
NC_000015.8:g.76681258_76681260delinsGCA	NCBI36
NG_016143.1:g.24433_24435delinsTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.779_781delinsTGC MANE Select	ENSP00000315602.5:p.Val260=
ENST00000326828.5:c.779_781delinsTGC	ENSP00000315602.5:p.Val260=
ENST00000348639.7:c.779_781delinsTGC	ENSP00000267951.4:p.Val260=
ENST00000558903.1:n.486_488delinsTGC
ENST00000559658.5:c.779_781delinsTGC	ENSP00000452896.1:p.Val260=
NM_000743.4:c.779_781delinsTGC	NP_000734.2:p.Val260=
NM_001166694.1:c.779_781delinsTGC	NP_001160166.1:p.Val260=
NR_046313.1:n.1280_1282delinsTGC
XM_006720382.1:c.578_580delinsTGC	XP_006720445.1:p.Val193=
XM_011521173.1:c.698_700delinsTGC	XP_011519475.1:p.Val233=
XM_006720382.3:c.578_580delinsTGC	XP_006720445.1:p.Val193=
NM_000743.5:c.779_781delinsTGC MANE Select	NP_000734.2:p.Val260=
NM_001166694.2:c.779_781delinsTGC	NP_001160166.1:p.Val260=
NR_046313.2:n.981_983delinsTGC