Canonical Allele Identifier: CA2761148024
Gene: CHRNA9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354475del , CM000666.2:g.40354475del GRCh38
NC_000004.11:g.40356492del , CM000666.1:g.40356492del GRCh37
NC_000004.10:g.40051249del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1395del MANE Select ENSP00000312663.2:p.Met466TrpfsTer4
ENST00000310169.2:c.1395del ENSP00000312663.2:p.Met466TrpfsTer4
NM_017581.3:c.1395del NP_060051.2:p.Met466TrpfsTer4
NM_017581.4:c.1395del MANE Select NP_060051.2:p.Met466TrpfsTer4
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Search 100 bp 3'