Canonical Allele Identifier: CA2129502793
Gene: PAX9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663369_36663375delinsCTACTCG , CM000676.2:g.36663369_36663375delinsCTACTCG GRCh38
NC_000014.8:g.37132574_37132580delinsCTACTCG , CM000676.1:g.37132574_37132580delinsCTACTCG GRCh37
NC_000014.7:g.36202325_36202331delinsCTACTCG NCBI36
NG_013357.1:g.10802_10808delinsCTACTCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.477_483delinsCTACTCG MANE Select ENSP00000355245.6:p.Ile159=
ENST00000361487.6:c.477_483delinsCTACTCG ENSP00000355245.6:p.Ile159=
ENST00000402703.6:c.477_483delinsCTACTCG ENSP00000384817.2:p.Ile159=
ENST00000554201.1:c.-85_-79delinsCTACTCG ENSP00000450434.1:n.-85_-79delinsCTACTCG
NM_006194.3:c.477_483delinsCTACTCG NP_006185.1:p.Ile159=
NM_001372076.1:c.477_483delinsCTACTCG MANE Select NP_001359005.1:p.Ile159=
NM_006194.4:c.477_483delinsCTACTCG NP_006185.1:p.Ile159=
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