Canonical Allele Identifier: CA2129502914
Gene: PAX9 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663426G= , CM000676.2:g.36663426G= GRCh38
NC_000014.8:g.37132631G= , CM000676.1:g.37132631G= GRCh37
NC_000014.7:g.36202382G= NCBI36
NG_013357.1:g.10859G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.534G= MANE Select ENSP00000355245.6:p.Gly178=
ENST00000361487.6:c.534G= ENSP00000355245.6:p.Gly178=
ENST00000402703.6:c.534G= ENSP00000384817.2:p.Gly178=
ENST00000554201.1:c.-28G= ENSP00000450434.1:n.-28G=
NM_006194.3:c.534G= NP_006185.1:p.Gly178=
NM_001372076.1:c.534G= MANE Select NP_001359005.1:p.Gly178=
NM_006194.4:c.534G= NP_006185.1:p.Gly178=
Search 100 bp 5'
Search 100 bp 3'