Canonical Allele Identifier: CA389466149
Gene: PAX9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663011G>C , CM000676.2:g.36663011G>C GRCh38
NC_000014.8:g.37132216G>C , CM000676.1:g.37132216G>C GRCh37
NC_000014.7:g.36201967G>C NCBI36
NG_013357.1:g.10444G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.119G>C MANE Select ENSP00000355245.6:p.Cys40Ser
ENST00000555639.2:c.119G>C ENSP00000501203.1:p.Cys40Ser
ENST00000361487.6:c.119G>C ENSP00000355245.6:p.Cys40Ser
ENST00000402703.6:c.119G>C ENSP00000384817.2:p.Cys40Ser
ENST00000554201.1:c.-443G>C ENSP00000450434.1:n.-443G>C
ENST00000555639.1:n.421G>C
NM_006194.3:c.119G>C NP_006185.1:p.Cys40Ser
NM_001372076.1:c.119G>C MANE Select NP_001359005.1:p.Cys40Ser
NM_006194.4:c.119G>C NP_006185.1:p.Cys40Ser