Canonical Allele Identifier: CA2129502686
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663319T= , CM000676.2:g.36663319T= GRCh38
NC_000014.8:g.37132524T= , CM000676.1:g.37132524T= GRCh37
NC_000014.7:g.36202275T= NCBI36
NG_013357.1:g.10752T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.427T= MANE Select ENSP00000355245.6:p.Tyr143=
ENST00000361487.6:c.427T= ENSP00000355245.6:p.Tyr143=
ENST00000402703.6:c.427T= ENSP00000384817.2:p.Tyr143=
ENST00000554201.1:c.-135T= ENSP00000450434.1:n.-135T=
NM_006194.3:c.427T= NP_006185.1:p.Tyr143=
NM_001372076.1:c.427T= MANE Select NP_001359005.1:p.Tyr143=
NM_006194.4:c.427T= NP_006185.1:p.Tyr143=