Canonical Allele Identifier: CA2801203461
Gene: PAX9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663358_36663360del , CM000676.2:g.36663358_36663360del GRCh38
NC_000014.8:g.37132563_37132565del , CM000676.1:g.37132563_37132565del GRCh37
NC_000014.7:g.36202314_36202316del NCBI36
NG_013357.1:g.10791_10793del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.466_468del MANE Select ENSP00000355245.6:p.Tyr156del
ENST00000361487.6:c.466_468del ENSP00000355245.6:p.Tyr156del
ENST00000402703.6:c.466_468del ENSP00000384817.2:p.Tyr156del
ENST00000554201.1:c.-96_-94del ENSP00000450434.1:n.-96_-94del
NM_006194.3:c.466_468del NP_006185.1:p.Tyr156del
NM_001372076.1:c.466_468del MANE Select NP_001359005.1:p.Tyr156del
NM_006194.4:c.466_468del NP_006185.1:p.Tyr156del
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