Canonical Allele Identifier: CA2129502394
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663078G= , CM000676.2:g.36663078G= GRCh38
NC_000014.8:g.37132283G= , CM000676.1:g.37132283G= GRCh37
NC_000014.7:g.36202034G= NCBI36
NG_013357.1:g.10511G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.186G= MANE Select ENSP00000355245.6:p.Glu62=
ENST00000555639.2:c.186G= ENSP00000501203.1:p.Glu62=
ENST00000361487.6:c.186G= ENSP00000355245.6:p.Glu62=
ENST00000402703.6:c.186G= ENSP00000384817.2:p.Glu62=
ENST00000554201.1:c.-376G= ENSP00000450434.1:n.-376G=
ENST00000555639.1:n.488G=
NM_006194.3:c.186G= NP_006185.1:p.Glu62=
NM_001372076.1:c.186G= MANE Select NP_001359005.1:p.Glu62=
NM_006194.4:c.186G= NP_006185.1:p.Glu62=