Canonical Allele Identifier: CA2129502452
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663136A= , CM000676.2:g.36663136A= GRCh38
NC_000014.8:g.37132341A= , CM000676.1:g.37132341A= GRCh37
NC_000014.7:g.36202092A= NCBI36
NG_013357.1:g.10569A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.244A= MANE Select ENSP00000355245.6:p.Thr82=
ENST00000555639.2:c.244A= ENSP00000501203.1:p.Thr82=
ENST00000361487.6:c.244A= ENSP00000355245.6:p.Thr82=
ENST00000402703.6:c.244A= ENSP00000384817.2:p.Thr82=
ENST00000554201.1:c.-318A= ENSP00000450434.1:n.-318A=
ENST00000555639.1:n.546A=
NM_006194.3:c.244A= NP_006185.1:p.Thr82=
NM_001372076.1:c.244A= MANE Select NP_001359005.1:p.Thr82=
NM_006194.4:c.244A= NP_006185.1:p.Thr82=