Canonical Allele Identifier: CA2129502529
Gene: PAX9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663212T= , CM000676.2:g.36663212T= GRCh38
NC_000014.8:g.37132417T= , CM000676.1:g.37132417T= GRCh37
NC_000014.7:g.36202168T= NCBI36
NG_013357.1:g.10645T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.320T= MANE Select ENSP00000355245.6:p.Leu107=
ENST00000361487.6:c.320T= ENSP00000355245.6:p.Leu107=
ENST00000402703.6:c.320T= ENSP00000384817.2:p.Leu107=
ENST00000554201.1:c.-242T= ENSP00000450434.1:n.-242T=
NM_006194.3:c.320T= NP_006185.1:p.Leu107=
NM_001372076.1:c.320T= MANE Select NP_001359005.1:p.Leu107=
NM_006194.4:c.320T= NP_006185.1:p.Leu107=
Search 100 bp 5'
Search 100 bp 3'