Canonical Allele Identifier: CA2189590226

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601933_78601936delinsTGTA , CM000677.2:g.78601933_78601936delinsTGTA	GRCh38
NC_000015.9:g.78894275_78894278delinsTGTA , CM000677.1:g.78894275_78894278delinsTGTA	GRCh37
NC_000015.8:g.76681330_76681333delinsTGTA	NCBI36
NG_016143.1:g.24360_24363delinsTACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.706_709delinsTACA MANE Select	ENSP00000315602.5:p.Tyr236=
ENST00000326828.5:c.706_709delinsTACA	ENSP00000315602.5:p.Tyr236=
ENST00000348639.7:c.706_709delinsTACA	ENSP00000267951.4:p.Tyr236=
ENST00000558903.1:n.413_416delinsTACA
ENST00000559658.5:c.706_709delinsTACA	ENSP00000452896.1:p.Tyr236=
NM_000743.4:c.706_709delinsTACA	NP_000734.2:p.Tyr236=
NM_001166694.1:c.706_709delinsTACA	NP_001160166.1:p.Tyr236=
NR_046313.1:n.1207_1210delinsTACA
XM_006720382.1:c.505_508delinsTACA	XP_006720445.1:p.Tyr169=
XM_011521173.1:c.625_628delinsTACA	XP_011519475.1:p.Tyr209=
XM_006720382.3:c.505_508delinsTACA	XP_006720445.1:p.Tyr169=
NM_000743.5:c.706_709delinsTACA MANE Select	NP_000734.2:p.Tyr236=
NM_001166694.2:c.706_709delinsTACA	NP_001160166.1:p.Tyr236=
NR_046313.2:n.908_911delinsTACA