Canonical Allele Identifier: CA2695212815
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663148_36663154dup , CM000676.2:g.36663148_36663154dup GRCh38
NC_000014.8:g.37132353_37132359dup , CM000676.1:g.37132353_37132359dup GRCh37
NC_000014.7:g.36202104_36202110dup NCBI36
NG_013357.1:g.10581_10587dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.256_262dup MANE Select ENSP00000355245.6:p.Arg88ProfsTer?
ENST00000361487.6:c.256_262dup ENSP00000355245.6:p.Arg88ProfsTer?
ENST00000402703.6:c.256_262dup ENSP00000384817.2:p.Arg88ProfsTer?
ENST00000554201.1:c.-306_-300dup ENSP00000450434.1:n.-306_-300dup
NM_006194.3:c.256_262dup NP_006185.1:p.Arg88ProfsTer?
NM_001372076.1:c.256_262dup MANE Select NP_001359005.1:p.Arg88ProfsTer?
NM_006194.4:c.256_262dup NP_006185.1:p.Arg88ProfsTer?