Canonical Allele Identifier: CA2129502819
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663386C= , CM000676.2:g.36663386C= GRCh38
NC_000014.8:g.37132591C= , CM000676.1:g.37132591C= GRCh37
NC_000014.7:g.36202342C= NCBI36
NG_013357.1:g.10819C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361487.7:c.494C= MANE Select ENSP00000355245.6:p.Pro165=
ENST00000361487.6:c.494C= ENSP00000355245.6:p.Pro165=
ENST00000402703.6:c.494C= ENSP00000384817.2:p.Pro165=
ENST00000554201.1:c.-68C= ENSP00000450434.1:n.-68C=
NM_006194.3:c.494C= NP_006185.1:p.Pro165=
NM_001372076.1:c.494C= MANE Select NP_001359005.1:p.Pro165=
NM_006194.4:c.494C= NP_006185.1:p.Pro165=