Canonical Allele Identifier: CA2129502957

Gene: PAX9

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.36663454A= , CM000676.2:g.36663454A=	GRCh38
NC_000014.8:g.37132659A= , CM000676.1:g.37132659A=	GRCh37
NC_000014.7:g.36202410A=	NCBI36
NG_013357.1:g.10887A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361487.7:c.562A= MANE Select	ENSP00000355245.6:p.Met188=
ENST00000361487.6:c.562A=	ENSP00000355245.6:p.Met188=
ENST00000402703.6:c.562A=	ENSP00000384817.2:p.Met188=
ENST00000554201.1:c.1A=	ENSP00000450434.1:p.Met1=
NM_006194.3:c.562A=	NP_006185.1:p.Met188=
NM_001372076.1:c.562A= MANE Select	NP_001359005.1:p.Met188=
NM_006194.4:c.562A=	NP_006185.1:p.Met188=