Canonical Allele Identifier: CA389466437
Gene: PAX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663145A>C , CM000676.2:g.36663145A>C GRCh38
NC_000014.8:g.37132350A>C , CM000676.1:g.37132350A>C GRCh37
NC_000014.7:g.36202101A>C NCBI36
NG_013357.1:g.10578A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.253A>C MANE Select ENSP00000355245.6:p.Lys85Gln
ENST00000361487.6:c.253A>C ENSP00000355245.6:p.Lys85Gln
ENST00000402703.6:c.253A>C ENSP00000384817.2:p.Lys85Gln
ENST00000554201.1:c.-309A>C ENSP00000450434.1:n.-309A>C
NM_006194.3:c.253A>C NP_006185.1:p.Lys85Gln
NM_001372076.1:c.253A>C MANE Select NP_001359005.1:p.Lys85Gln
NM_006194.4:c.253A>C NP_006185.1:p.Lys85Gln