Canonical Allele Identifier: CA2670423987
Gene: CHRNA9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354403del , CM000666.2:g.40354403del GRCh38
NC_000004.11:g.40356420del , CM000666.1:g.40356420del GRCh37
NC_000004.10:g.40051177del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1323del MANE Select ENSP00000312663.2:p.Asn442IlefsTer14
ENST00000310169.2:c.1323del ENSP00000312663.2:p.Asn442IlefsTer14
NM_017581.3:c.1323del NP_060051.2:p.Asn442IlefsTer14
NM_017581.4:c.1323del MANE Select NP_060051.2:p.Asn442IlefsTer14