Canonical Allele Identifier: CA389466090
Gene: PAX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36662981T>G , CM000676.2:g.36662981T>G GRCh38
NC_000014.8:g.37132186T>G , CM000676.1:g.37132186T>G GRCh37
NC_000014.7:g.36201937T>G NCBI36
NG_013357.1:g.10414T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.89T>G MANE Select ENSP00000355245.6:p.Val30Gly
ENST00000555639.2:c.89T>G ENSP00000501203.1:p.Val30Gly
ENST00000361487.6:c.89T>G ENSP00000355245.6:p.Val30Gly
ENST00000402703.6:c.89T>G ENSP00000384817.2:p.Val30Gly
ENST00000554201.1:c.-473T>G ENSP00000450434.1:n.-473T>G
ENST00000555639.1:n.391T>G
NM_006194.3:c.89T>G NP_006185.1:p.Val30Gly
NM_001372076.1:c.89T>G MANE Select NP_001359005.1:p.Val30Gly
NM_006194.4:c.89T>G NP_006185.1:p.Val30Gly