Canonical Allele Identifier: CA2129502414
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663102C= , CM000676.2:g.36663102C= GRCh38
NC_000014.8:g.37132307C= , CM000676.1:g.37132307C= GRCh37
NC_000014.7:g.36202058C= NCBI36
NG_013357.1:g.10535C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.210C= MANE Select ENSP00000355245.6:p.Ala70=
ENST00000555639.2:c.210C= ENSP00000501203.1:p.Ala70=
ENST00000361487.6:c.210C= ENSP00000355245.6:p.Ala70=
ENST00000402703.6:c.210C= ENSP00000384817.2:p.Ala70=
ENST00000554201.1:c.-352C= ENSP00000450434.1:n.-352C=
ENST00000555639.1:n.512C=
NM_006194.3:c.210C= NP_006185.1:p.Ala70=
NM_001372076.1:c.210C= MANE Select NP_001359005.1:p.Ala70=
NM_006194.4:c.210C= NP_006185.1:p.Ala70=