Canonical Allele Identifier: CA14026450

Gene: PAX9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36673764C>A , CM000676.2:g.36673764C>A	GRCh38
NC_000014.8:g.37142969C>A , CM000676.1:g.37142969C>A	GRCh37
NC_000014.7:g.36212720C>A	NCBI36
NG_013357.1:g.21197C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361487.7:c.772-2434C>A MANE Select	ENSP00000355245.6:n.772-2434C>A
ENST00000361487.6:c.772-2434C>A	ENSP00000355245.6:n.772-2434C>A
ENST00000402703.6:c.772-2434C>A	ENSP00000384817.2:n.772-2434C>A
ENST00000554201.1:c.201-2434C>A	ENSP00000450434.1:n.201-2434C>A
ENST00000557107.1:n.837+1655C>A
NM_006194.3:c.772-2434C>A	NP_006185.1:n.772-2434C>A
NM_001372076.1:c.772-2434C>A MANE Select	NP_001359005.1:n.772-2434C>A
NM_006194.4:c.772-2434C>A	NP_006185.1:n.772-2434C>A