Canonical Allele Identifier: CA2189591391

Gene: CHRNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602448_78602452delinsGCTCC , CM000677.2:g.78602448_78602452delinsGCTCC	GRCh38
NC_000015.9:g.78894790_78894794delinsGCTCC , CM000677.1:g.78894790_78894794delinsGCTCC	GRCh37
NC_000015.8:g.76681845_76681849delinsGCTCC	NCBI36
NG_016143.1:g.23844_23848delinsGGAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.378-188_378-184delinsGGAGC MANE Select	ENSP00000315602.5:n.378-188_378-184delinsGGAGC
ENST00000326828.5:c.378-188_378-184delinsGGAGC	ENSP00000315602.5:n.378-188_378-184delinsGGAGC
ENST00000348639.7:c.378-188_378-184delinsGGAGC	ENSP00000267951.4:n.378-188_378-184delinsGGAGC
ENST00000558903.1:n.85-188_85-184delinsGGAGC
ENST00000559658.5:c.378-188_378-184delinsGGAGC	ENSP00000452896.1:n.378-188_378-184delinsGGAGC
NM_000743.4:c.378-188_378-184delinsGGAGC	NP_000734.2:n.378-188_378-184delinsGGAGC
NM_001166694.1:c.378-188_378-184delinsGGAGC	NP_001160166.1:n.378-188_378-184delinsGGAGC
NR_046313.1:n.879-188_879-184delinsGGAGC
XM_006720382.1:c.177-188_177-184delinsGGAGC	XP_006720445.1:n.177-188_177-184delinsGGAGC
XM_011521173.1:c.297-188_297-184delinsGGAGC	XP_011519475.1:n.297-188_297-184delinsGGAGC
XM_006720382.3:c.177-188_177-184delinsGGAGC	XP_006720445.1:n.177-188_177-184delinsGGAGC
NM_000743.5:c.378-188_378-184delinsGGAGC MANE Select	NP_000734.2:n.378-188_378-184delinsGGAGC
NM_001166694.2:c.378-188_378-184delinsGGAGC	NP_001160166.1:n.378-188_378-184delinsGGAGC
NR_046313.2:n.580-188_580-184delinsGGAGC