Canonical Allele Identifier: CA1452584476
Gene: CHRNA9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.40354436_40354437delinsGA , CM000666.2:g.40354436_40354437delinsGA GRCh38
NC_000004.11:g.40356453_40356454delinsGA , CM000666.1:g.40356453_40356454delinsGA GRCh37
NC_000004.10:g.40051210_40051211delinsGA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000310169.3:c.1356_1357delinsGA MANE Select ENSP00000312663.2:p.Ala452=
ENST00000310169.2:c.1356_1357delinsGA ENSP00000312663.2:p.Ala452=
NM_017581.3:c.1356_1357delinsGA NP_060051.2:p.Ala452=
NM_017581.4:c.1356_1357delinsGA MANE Select NP_060051.2:p.Ala452=
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