Canonical Allele Identifier: CA2629793183
Gene: CHRNA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78595880del , CM000677.2:g.78595880del GRCh38
NC_000015.9:g.78888222del , CM000677.1:g.78888222del GRCh37
NC_000015.8:g.76675277del NCBI36
NG_016143.1:g.30416del
NG_023328.1:g.35361del

Transcript Alleles

HGVS Amino-acid Change
ENST00000326828.6:c.*724del MANE Select ENSP00000315602.5:n.*724del
ENST00000326828.5:c.*724del ENSP00000315602.5:n.*724del
ENST00000348639.7:c.1390-2689del ENSP00000267951.4:n.1390-2689del
ENST00000559002.5:n.193+660del
ENST00000559658.5:c.*64+660del ENSP00000452896.1:n.*64+660del
NM_000743.4:c.*724del NP_000734.2:n.*724del
NM_001166694.1:c.1390-2689del NP_001160166.1:n.1390-2689del
NR_046313.1:n.2083+660del
XM_006720382.1:c.*724del XP_006720445.1:n.*724del
XM_011521173.1:c.*724del XP_011519475.1:n.*724del
XM_006720382.3:c.*724del XP_006720445.1:n.*724del
NM_000743.5:c.*724del MANE Select NP_000734.2:n.*724del
NM_001166694.2:c.1390-2689del NP_001160166.1:n.1390-2689del
NR_046313.2:n.1784+660del