Canonical Allele Identifier: CA2129502503
Gene: PAX9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663182T= , CM000676.2:g.36663182T= GRCh38
NC_000014.8:g.37132387T= , CM000676.1:g.37132387T= GRCh37
NC_000014.7:g.36202138T= NCBI36
NG_013357.1:g.10615T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.290T= MANE Select ENSP00000355245.6:p.Ile97=
ENST00000361487.6:c.290T= ENSP00000355245.6:p.Ile97=
ENST00000402703.6:c.290T= ENSP00000384817.2:p.Ile97=
ENST00000554201.1:c.-272T= ENSP00000450434.1:n.-272T=
NM_006194.3:c.290T= NP_006185.1:p.Ile97=
NM_001372076.1:c.290T= MANE Select NP_001359005.1:p.Ile97=
NM_006194.4:c.290T= NP_006185.1:p.Ile97=
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