Canonical Allele Identifier: CA971782758
Gene: CHRNA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78601914_78601915insTCTCGGTGGTCGCCGTATCATTAA , CM000677.2:g.78601914_78601915insTCTCGGTGGTCGCCGTATCATTAA GRCh38
NC_000015.9:g.78894256_78894257insTCTCGGTGGTCGCCGTATCATTAA , CM000677.1:g.78894256_78894257insTCTCGGTGGTCGCCGTATCATTAA GRCh37
NC_000015.8:g.76681311_76681312insTCTCGGTGGTCGCCGTATCATTAA NCBI36
NG_016143.1:g.24382_24383insTAATGATACGGCGACCACCGAGAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.728_729insTAATGATACGGCGACCACCGAGAT MANE Select ENSP00000315602.5:p.Phe243_Tyr244insAsnAspThrAlaThrThrGluIle
ENST00000326828.5:c.728_729insTAATGATACGGCGACCACCGAGAT ENSP00000315602.5:p.Phe243_Tyr244insAsnAspThrAlaThrThrGluIle
ENST00000348639.7:c.728_729insTAATGATACGGCGACCACCGAGAT ENSP00000267951.4:p.Phe243_Tyr244insAsnAspThrAlaThrThrGluIle
ENST00000558903.1:n.435_436insTAATGATACGGCGACCACCGAGAT
ENST00000559658.5:c.728_729insTAATGATACGGCGACCACCGAGAT ENSP00000452896.1:p.Phe243_Tyr244insAsnAspThrAlaThrThrGluIle
NM_000743.4:c.728_729insTAATGATACGGCGACCACCGAGAT NP_000734.2:p.Phe243_Tyr244insAsnAspThrAlaThrThrGluIle
NM_001166694.1:c.728_729insTAATGATACGGCGACCACCGAGAT NP_001160166.1:p.Phe243_Tyr244insAsnAspThrAlaThrThrGluIle
NR_046313.1:n.1229_1230insTAATGATACGGCGACCACCGAGAT
XM_006720382.1:c.527_528insTAATGATACGGCGACCACCGAGAT XP_006720445.1:p.Phe176_Tyr177insAsnAspThrAlaThrThrGluIle
XM_011521173.1:c.647_648insTAATGATACGGCGACCACCGAGAT XP_011519475.1:p.Phe216_Tyr217insAsnAspThrAlaThrThrGluIle
XM_006720382.3:c.527_528insTAATGATACGGCGACCACCGAGAT XP_006720445.1:p.Phe176_Tyr177insAsnAspThrAlaThrThrGluIle
NM_000743.5:c.728_729insTAATGATACGGCGACCACCGAGAT MANE Select NP_000734.2:p.Phe243_Tyr244insAsnAspThrAlaThrThrGluIle
NM_001166694.2:c.728_729insTAATGATACGGCGACCACCGAGAT NP_001160166.1:p.Phe243_Tyr244insAsnAspThrAlaThrThrGluIle
NR_046313.2:n.930_931insTAATGATACGGCGACCACCGAGAT