Canonical Allele Identifier: CA2189589961

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601844_78601873delinsGGGCAGGTAGAAGACGAGCACAGTGAGGAA , CM000677.2:g.78601844_78601873delinsGGGCAGGTAGAAGACGAGCACAGTGAGGAA	GRCh38
NC_000015.9:g.78894186_78894215delinsGGGCAGGTAGAAGACGAGCACAGTGAGGAA , CM000677.1:g.78894186_78894215delinsGGGCAGGTAGAAGACGAGCACAGTGAGGAA	GRCh37
NC_000015.8:g.76681241_76681270delinsGGGCAGGTAGAAGACGAGCACAGTGAGGAA	NCBI36
NG_016143.1:g.24423_24452delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.769_798delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC MANE Select	ENSP00000315602.5:p.Phe257=
ENST00000326828.5:c.769_798delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC	ENSP00000315602.5:p.Phe257=
ENST00000348639.7:c.769_798delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC	ENSP00000267951.4:p.Phe257=
ENST00000558903.1:n.476_505delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC
ENST00000559658.5:c.769_798delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC	ENSP00000452896.1:p.Phe257=
NM_000743.4:c.769_798delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC	NP_000734.2:p.Phe257=
NM_001166694.1:c.769_798delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC	NP_001160166.1:p.Phe257=
NR_046313.1:n.1270_1299delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC
XM_006720382.1:c.568_597delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC	XP_006720445.1:p.Phe190=
XM_011521173.1:c.688_717delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC	XP_011519475.1:p.Phe230=
XM_006720382.3:c.568_597delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC	XP_006720445.1:p.Phe190=
NM_000743.5:c.769_798delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC MANE Select	NP_000734.2:p.Phe257=
NM_001166694.2:c.769_798delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC	NP_001160166.1:p.Phe257=
NR_046313.2:n.971_1000delinsTTCCTCACTGTGCTCGTCTTCTACCTGCCC