Canonical Allele Identifier: CA2629782963
Gene: CHRNA5 HGNC NCBI

Linked Data

gnomAD v4: 15-78565553-CTG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.78565554_78565555del , CM000677.2:g.78565554_78565555del GRCh38
NC_000015.9:g.78857896_78857897del , CM000677.1:g.78857896_78857897del GRCh37
NC_000015.8:g.76644951_76644952del NCBI36
NG_023328.1:g.5035_5036del

Transcript Alleles

HGVS Amino-acid change
ENST00000299565.9:c.-166_-165del MANE Select ENSP00000299565.5:n.-166_-165del
NM_000745.3:c.-166_-165del NP_000736.2:n.-166_-165del
NM_001307945.1:c.-166_-165del NP_001294874.1:n.-166_-165del
XM_005254142.2:c.-166_-165del XP_005254199.1:n.-166_-165del
NM_001307945.2:c.-166_-165del NP_001294874.1:n.-166_-165del
NM_000745.4:c.-166_-165del MANE Select NP_000736.2:n.-166_-165del
NM_001395171.1:c.-166_-165del NP_001382100.1:n.-166_-165del
NM_001395172.1:c.-166_-165del NP_001382101.1:n.-166_-165del
NM_001395173.1:c.-166_-165del NP_001382102.1:n.-166_-165del
NM_001395174.1:c.-166_-165del NP_001382103.1:n.-166_-165del
NM_001395175.1:c.-166_-165del NP_001382104.1:n.-166_-165del
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