Canonical Allele Identifier: CA389466756
Gene: PAX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663295G>C , CM000676.2:g.36663295G>C GRCh38
NC_000014.8:g.37132500G>C , CM000676.1:g.37132500G>C GRCh37
NC_000014.7:g.36202251G>C NCBI36
NG_013357.1:g.10728G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.403G>C MANE Select ENSP00000355245.6:p.Ala135Pro
ENST00000361487.6:c.403G>C ENSP00000355245.6:p.Ala135Pro
ENST00000402703.6:c.403G>C ENSP00000384817.2:p.Ala135Pro
ENST00000554201.1:c.-159G>C ENSP00000450434.1:n.-159G>C
NM_006194.3:c.403G>C NP_006185.1:p.Ala135Pro
NM_001372076.1:c.403G>C MANE Select NP_001359005.1:p.Ala135Pro
NM_006194.4:c.403G>C NP_006185.1:p.Ala135Pro