Canonical Allele Identifier: CA2189581320
Gene: CHRNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78596156_78596166delinsAATGGGTAACG , CM000677.2:g.78596156_78596166delinsAATGGGTAACG GRCh38
NC_000015.9:g.78888498_78888508delinsAATGGGTAACG , CM000677.1:g.78888498_78888508delinsAATGGGTAACG GRCh37
NC_000015.8:g.76675553_76675563delinsAATGGGTAACG NCBI36
NG_016143.1:g.30130_30140delinsCGTTACCCATT
NG_023328.1:g.35637_35647delinsAATGGGTAACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.*438_*448delinsCGTTACCCATT MANE Select ENSP00000315602.5:n.*438_*448delinsCGTTACCCATT
ENST00000326828.5:c.*438_*448delinsCGTTACCCATT ENSP00000315602.5:n.*438_*448delinsCGTTACCCATT
ENST00000348639.7:c.1390-2975_1390-2965delinsCGTTACCCATT ENSP00000267951.4:n.1390-2975_1390-2965delinsCGTTACCCATT
ENST00000559002.5:n.193+374_193+384delinsCGTTACCCATT
ENST00000559658.5:c.*64+374_*64+384delinsCGTTACCCATT ENSP00000452896.1:n.*64+374_*64+384delinsCGTTACCCATT
NM_000743.4:c.*438_*448delinsCGTTACCCATT NP_000734.2:n.*438_*448delinsCGTTACCCATT
NM_001166694.1:c.1390-2975_1390-2965delinsCGTTACCCATT NP_001160166.1:n.1390-2975_1390-2965delinsCGTTACCCATT
NR_046313.1:n.2083+374_2083+384delinsCGTTACCCATT
XM_006720382.1:c.*438_*448delinsCGTTACCCATT XP_006720445.1:n.*438_*448delinsCGTTACCCATT
XM_011521173.1:c.*438_*448delinsCGTTACCCATT XP_011519475.1:n.*438_*448delinsCGTTACCCATT
XM_006720382.3:c.*438_*448delinsCGTTACCCATT XP_006720445.1:n.*438_*448delinsCGTTACCCATT
NM_000743.5:c.*438_*448delinsCGTTACCCATT MANE Select NP_000734.2:n.*438_*448delinsCGTTACCCATT
NM_001166694.2:c.1390-2975_1390-2965delinsCGTTACCCATT NP_001160166.1:n.1390-2975_1390-2965delinsCGTTACCCATT
NR_046313.2:n.1784+374_1784+384delinsCGTTACCCATT