Canonical Allele Identifier: CA2129502506
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663186C= , CM000676.2:g.36663186C= GRCh38
NC_000014.8:g.37132391C= , CM000676.1:g.37132391C= GRCh37
NC_000014.7:g.36202142C= NCBI36
NG_013357.1:g.10619C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.294C= MANE Select ENSP00000355245.6:p.Phe98=
ENST00000361487.6:c.294C= ENSP00000355245.6:p.Phe98=
ENST00000402703.6:c.294C= ENSP00000384817.2:p.Phe98=
ENST00000554201.1:c.-268C= ENSP00000450434.1:n.-268C=
NM_006194.3:c.294C= NP_006185.1:p.Phe98=
NM_001372076.1:c.294C= MANE Select NP_001359005.1:p.Phe98=
NM_006194.4:c.294C= NP_006185.1:p.Phe98=