Canonical Allele Identifier: CA2695212812
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663103dup , CM000676.2:g.36663103dup GRCh38
NC_000014.8:g.37132308dup , CM000676.1:g.37132308dup GRCh37
NC_000014.7:g.36202059dup NCBI36
NG_013357.1:g.10536dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.211dup MANE Select ENSP00000355245.6:p.Ile71AsnfsTer?
ENST00000555639.2:c.211dup ENSP00000501203.1:p.Ile71AsnfsTer?
ENST00000361487.6:c.211dup ENSP00000355245.6:p.Ile71AsnfsTer?
ENST00000402703.6:c.211dup ENSP00000384817.2:p.Ile71AsnfsTer?
ENST00000554201.1:c.-351dup ENSP00000450434.1:n.-351dup
ENST00000555639.1:n.513dup
NM_006194.3:c.211dup NP_006185.1:p.Ile71AsnfsTer?
NM_001372076.1:c.211dup MANE Select NP_001359005.1:p.Ile71AsnfsTer?
NM_006194.4:c.211dup NP_006185.1:p.Ile71AsnfsTer?