Canonical Allele Identifier: CA645583582

Gene: CHRNA3

Linked Data

• COSMIC: COSM5383883

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78602142_78602143delinsAA , CM000677.2:g.78602142_78602143delinsAA	GRCh38
NC_000015.9:g.78894484_78894485delinsAA , CM000677.1:g.78894484_78894485delinsAA	GRCh37
NC_000015.8:g.76681539_76681540delinsAA	NCBI36
NG_016143.1:g.24153_24154delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326828.6:c.499_500delinsTT MANE Select	ENSP00000315602.5:p.Pro167Leu
ENST00000326828.5:c.499_500delinsTT	ENSP00000315602.5:p.Pro167Leu
ENST00000348639.7:c.499_500delinsTT	ENSP00000267951.4:p.Pro167Leu
ENST00000558903.1:n.206_207delinsTT
ENST00000559658.5:c.499_500delinsTT	ENSP00000452896.1:p.Pro167Leu
NM_000743.4:c.499_500delinsTT	NP_000734.2:p.Pro167Leu
NM_001166694.1:c.499_500delinsTT	NP_001160166.1:p.Pro167Leu
NR_046313.1:n.1000_1001delinsTT
XM_006720382.1:c.298_299delinsTT	XP_006720445.1:p.Pro100Leu
XM_011521173.1:c.418_419delinsTT	XP_011519475.1:p.Pro140Leu
XM_006720382.3:c.298_299delinsTT	XP_006720445.1:p.Pro100Leu
NM_000743.5:c.499_500delinsTT MANE Select	NP_000734.2:p.Pro167Leu
NM_001166694.2:c.499_500delinsTT	NP_001160166.1:p.Pro167Leu
NR_046313.2:n.701_702delinsTT