Canonical Allele Identifier: CA389467122
Gene: PAX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663472T>G , CM000676.2:g.36663472T>G GRCh38
NC_000014.8:g.37132677T>G , CM000676.1:g.37132677T>G GRCh37
NC_000014.7:g.36202428T>G NCBI36
NG_013357.1:g.10905T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000361487.7:c.580T>G MANE Select ENSP00000355245.6:p.Ser194Ala
ENST00000361487.6:c.580T>G ENSP00000355245.6:p.Ser194Ala
ENST00000402703.6:c.580T>G ENSP00000384817.2:p.Ser194Ala
ENST00000554201.1:c.19T>G ENSP00000450434.1:p.Ser7Ala
NM_006194.3:c.580T>G NP_006185.1:p.Ser194Ala
NM_001372076.1:c.580T>G MANE Select NP_001359005.1:p.Ser194Ala
NM_006194.4:c.580T>G NP_006185.1:p.Ser194Ala