Canonical Allele Identifier: CA2670423988
Gene: CHRNA9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354464_40354466del , CM000666.2:g.40354464_40354466del GRCh38
NC_000004.11:g.40356481_40356483del , CM000666.1:g.40356481_40356483del GRCh37
NC_000004.10:g.40051238_40051240del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1384_1386del MANE Select ENSP00000312663.2:p.Ile462del
ENST00000310169.2:c.1384_1386del ENSP00000312663.2:p.Ile462del
NM_017581.3:c.1384_1386del NP_060051.2:p.Ile462del
NM_017581.4:c.1384_1386del MANE Select NP_060051.2:p.Ile462del