Canonical Allele Identifier: CA2695212817
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663214dup , CM000676.2:g.36663214dup GRCh38
NC_000014.8:g.37132419dup , CM000676.1:g.37132419dup GRCh37
NC_000014.7:g.36202170dup NCBI36
NG_013357.1:g.10647dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.322dup MANE Select ENSP00000355245.6:p.Ala108GlyfsTer?
ENST00000361487.6:c.322dup ENSP00000355245.6:p.Ala108GlyfsTer?
ENST00000402703.6:c.322dup ENSP00000384817.2:p.Ala108GlyfsTer?
ENST00000554201.1:c.-240dup ENSP00000450434.1:n.-240dup
NM_006194.3:c.322dup NP_006185.1:p.Ala108GlyfsTer?
NM_001372076.1:c.322dup MANE Select NP_001359005.1:p.Ala108GlyfsTer?
NM_006194.4:c.322dup NP_006185.1:p.Ala108GlyfsTer?