Canonical Allele Identifier: CA1452584487
Gene: CHRNA9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354447_40354448delinsAC , CM000666.2:g.40354447_40354448delinsAC GRCh38
NC_000004.11:g.40356464_40356465delinsAC , CM000666.1:g.40356464_40356465delinsAC GRCh37
NC_000004.10:g.40051221_40051222delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000310169.3:c.1367_1368delinsAC MANE Select ENSP00000312663.2:p.Asp456=
ENST00000310169.2:c.1367_1368delinsAC ENSP00000312663.2:p.Asp456=
NM_017581.3:c.1367_1368delinsAC NP_060051.2:p.Asp456=
NM_017581.4:c.1367_1368delinsAC MANE Select NP_060051.2:p.Asp456=
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