Canonical Allele Identifier: CA389466136
Gene: PAX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663005G>A , CM000676.2:g.36663005G>A GRCh38
NC_000014.8:g.37132210G>A , CM000676.1:g.37132210G>A GRCh37
NC_000014.7:g.36201961G>A NCBI36
NG_013357.1:g.10438G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.113G>A MANE Select ENSP00000355245.6:p.Arg38Gln
ENST00000555639.2:c.113G>A ENSP00000501203.1:p.Arg38Gln
ENST00000361487.6:c.113G>A ENSP00000355245.6:p.Arg38Gln
ENST00000402703.6:c.113G>A ENSP00000384817.2:p.Arg38Gln
ENST00000554201.1:c.-449G>A ENSP00000450434.1:n.-449G>A
ENST00000555639.1:n.415G>A
NM_006194.3:c.113G>A NP_006185.1:p.Arg38Gln
NM_001372076.1:c.113G>A MANE Select NP_001359005.1:p.Arg38Gln
NM_006194.4:c.113G>A NP_006185.1:p.Arg38Gln