Canonical Allele Identifier: CA2575509803
Gene: PAX9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663572_36663579dup , CM000676.2:g.36663572_36663579dup GRCh38
NC_000014.8:g.37132777_37132784dup , CM000676.1:g.37132777_37132784dup GRCh37
NC_000014.7:g.36202528_36202535dup NCBI36
NG_013357.1:g.11005_11012dup

Transcript Alleles

HGVS Amino-acid change
ENST00000361487.7:c.631+49_631+56dup MANE Select ENSP00000355245.6:n.631+49_631+56dup
ENST00000361487.6:c.631+49_631+56dup ENSP00000355245.6:n.631+49_631+56dup
ENST00000402703.6:c.631+49_631+56dup ENSP00000384817.2:n.631+49_631+56dup
ENST00000554201.1:c.70+49_70+56dup ENSP00000450434.1:n.70+49_70+56dup
NM_006194.3:c.631+49_631+56dup NP_006185.1:n.631+49_631+56dup
NM_001372076.1:c.631+49_631+56dup MANE Select NP_001359005.1:n.631+49_631+56dup
NM_006194.4:c.631+49_631+56dup NP_006185.1:n.631+49_631+56dup