Canonical Allele Identifier: CA2629793148
Gene: CHRNA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78595872_78595873del , CM000677.2:g.78595872_78595873del GRCh38
NC_000015.9:g.78888214_78888215del , CM000677.1:g.78888214_78888215del GRCh37
NC_000015.8:g.76675269_76675270del NCBI36
NG_016143.1:g.30425_30426del
NG_023328.1:g.35353_35354del

Transcript Alleles

HGVS Amino-acid change
ENST00000326828.6:c.*733_*734del MANE Select ENSP00000315602.5:n.*733_*734del
ENST00000326828.5:c.*733_*734del ENSP00000315602.5:n.*733_*734del
ENST00000348639.7:c.1390-2680_1390-2679del ENSP00000267951.4:n.1390-2680_1390-2679del
ENST00000559002.5:n.193+669_193+670del
ENST00000559658.5:c.*64+669_*64+670del ENSP00000452896.1:n.*64+669_*64+670del
NM_000743.4:c.*733_*734del NP_000734.2:n.*733_*734del
NM_001166694.1:c.1390-2680_1390-2679del NP_001160166.1:n.1390-2680_1390-2679del
NR_046313.1:n.2083+669_2083+670del
XM_006720382.1:c.*733_*734del XP_006720445.1:n.*733_*734del
XM_011521173.1:c.*733_*734del XP_011519475.1:n.*733_*734del
XM_006720382.3:c.*733_*734del XP_006720445.1:n.*733_*734del
NM_000743.5:c.*733_*734del MANE Select NP_000734.2:n.*733_*734del
NM_001166694.2:c.1390-2680_1390-2679del NP_001160166.1:n.1390-2680_1390-2679del
NR_046313.2:n.1784+669_1784+670del