Canonical Allele Identifier: CA389465925
Gene: PAX9 HGNC NCBI

Linked Data

dbSNP Id: rs1418777481

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36662903C>A , CM000676.2:g.36662903C>A GRCh38
NC_000014.8:g.37132108C>A , CM000676.1:g.37132108C>A GRCh37
NC_000014.7:g.36201859C>A NCBI36
NG_013357.1:g.10336C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.11C>A MANE Select ENSP00000355245.6:p.Ala4Asp
ENST00000555639.2:c.11C>A ENSP00000501203.1:p.Ala4Asp
ENST00000361487.6:c.11C>A ENSP00000355245.6:p.Ala4Asp
ENST00000402703.6:c.11C>A ENSP00000384817.2:p.Ala4Asp
ENST00000554201.1:c.-551C>A ENSP00000450434.1:n.-551C>A
ENST00000555639.1:n.313C>A
NM_006194.3:c.11C>A NP_006185.1:p.Ala4Asp
NM_001372076.1:c.11C>A MANE Select NP_001359005.1:p.Ala4Asp
NM_006194.4:c.11C>A NP_006185.1:p.Ala4Asp