Canonical Allele Identifier: CA2670423982
Gene: CHRNA9 HGNC NCBI

Linked Data

gnomAD v4: 4-40354302-GGT-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354303_40354304del , CM000666.2:g.40354303_40354304del GRCh38
NC_000004.11:g.40356320_40356321del , CM000666.1:g.40356320_40356321del GRCh37
NC_000004.10:g.40051077_40051078del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1223_1224del MANE Select ENSP00000312663.2:p.Gly408GlufsTer21
ENST00000310169.2:c.1223_1224del ENSP00000312663.2:p.Gly408GlufsTer21
NM_017581.3:c.1223_1224del NP_060051.2:p.Gly408GlufsTer21
NM_017581.4:c.1223_1224del MANE Select NP_060051.2:p.Gly408GlufsTer21
Search 100 bp 5'
Search 100 bp 3'