Canonical Allele Identifier: CA2189590253

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78601938_78601941delinsAGCG , CM000677.2:g.78601938_78601941delinsAGCG	GRCh38
NC_000015.9:g.78894280_78894283delinsAGCG , CM000677.1:g.78894280_78894283delinsAGCG	GRCh37
NC_000015.8:g.76681335_76681338delinsAGCG	NCBI36
NG_016143.1:g.24355_24358delinsCGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.701_704delinsCGCT MANE Select	ENSP00000315602.5:p.Ser234=
ENST00000326828.5:c.701_704delinsCGCT	ENSP00000315602.5:p.Ser234=
ENST00000348639.7:c.701_704delinsCGCT	ENSP00000267951.4:p.Ser234=
ENST00000558903.1:n.408_411delinsCGCT
ENST00000559658.5:c.701_704delinsCGCT	ENSP00000452896.1:p.Ser234=
NM_000743.4:c.701_704delinsCGCT	NP_000734.2:p.Ser234=
NM_001166694.1:c.701_704delinsCGCT	NP_001160166.1:p.Ser234=
NR_046313.1:n.1202_1205delinsCGCT
XM_006720382.1:c.500_503delinsCGCT	XP_006720445.1:p.Ser167=
XM_011521173.1:c.620_623delinsCGCT	XP_011519475.1:p.Ser207=
XM_006720382.3:c.500_503delinsCGCT	XP_006720445.1:p.Ser167=
NM_000743.5:c.701_704delinsCGCT MANE Select	NP_000734.2:p.Ser234=
NM_001166694.2:c.701_704delinsCGCT	NP_001160166.1:p.Ser234=
NR_046313.2:n.903_906delinsCGCT