Canonical Allele Identifier: CA486097686

Gene: PAX9

Linked Data

• MyVariant Identifiers: chr14:g.37132272C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36663067C>A , CM000676.2:g.36663067C>A	GRCh38
NC_000014.8:g.37132272C>A , CM000676.1:g.37132272C>A	GRCh37
NC_000014.7:g.36202023C>A	NCBI36
NG_013357.1:g.10500C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361487.7:c.175C>A MANE Select	ENSP00000355245.6:p.Arg59=
ENST00000555639.2:c.175C>A	ENSP00000501203.1:p.Arg59=
ENST00000361487.6:c.175C>A	ENSP00000355245.6:p.Arg59=
ENST00000402703.6:c.175C>A	ENSP00000384817.2:p.Arg59=
ENST00000554201.1:c.-387C>A	ENSP00000450434.1:n.-387C>A
ENST00000555639.1:n.477C>A
NM_006194.3:c.175C>A	NP_006185.1:p.Arg59=
NM_001372076.1:c.175C>A MANE Select	NP_001359005.1:p.Arg59=
NM_006194.4:c.175C>A	NP_006185.1:p.Arg59=