Canonical Allele Identifier: CA389466477
Gene: PAX9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.37132368A>T (hg19) chr14:g.36663163A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.36663163A>T , CM000676.2:g.36663163A>T GRCh38
NC_000014.8:g.37132368A>T , CM000676.1:g.37132368A>T GRCh37
NC_000014.7:g.36202119A>T NCBI36
NG_013357.1:g.10596A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361487.7:c.271A>T MANE Select ENSP00000355245.6:p.Lys91Ter
ENST00000361487.6:c.271A>T ENSP00000355245.6:p.Lys91Ter
ENST00000402703.6:c.271A>T ENSP00000384817.2:p.Lys91Ter
ENST00000554201.1:c.-291A>T ENSP00000450434.1:n.-291A>T
NM_006194.3:c.271A>T NP_006185.1:p.Lys91Ter
NM_001372076.1:c.271A>T MANE Select NP_001359005.1:p.Lys91Ter
NM_006194.4:c.271A>T NP_006185.1:p.Lys91Ter
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