Canonical Allele Identifier: CA524638

Gene: ATAD3B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1485086T>A , CM000663.2:g.1485086T>A	GRCh38
NC_000001.10:g.1420466T>A , CM000663.1:g.1420466T>A	GRCh37
NC_000001.9:g.1410329T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_031921.6:c.821T>A MANE Select	NP_114127.3:p.Phe274Tyr
ENST00000673477.1:c.821T>A MANE Select	ENSP00000500094.1:p.Phe274Tyr
NM_001317238.1:c.683T>A	NP_001304167.1:p.Phe228Tyr
NM_001317238.2:c.683T>A	NP_001304167.1:p.Phe228Tyr
NM_031921.4:c.821T>A	NP_114127.3:p.Phe274Tyr
NM_031921.5:c.821T>A	NP_114127.3:p.Phe274Tyr
ENST00000308647.7:c.821T>A	ENSP00000311766.7:p.Phe274Tyr
ENST00000308647.8:c.503T>A	ENSP00000311766.8:p.Phe168Tyr
ENST00000472194.6:n.1157T>A
ENST00000474481.1:n.518T>A
ENST00000485748.5:n.1602T>A
XM_005244806.2:c.821T>A	XP_005244863.1:p.Phe274Tyr
XM_005244806.3:c.821T>A	XP_005244863.1:p.Phe274Tyr
XM_005244808.2:c.821T>A	XP_005244865.1:p.Phe274Tyr
XM_011542240.1:c.821T>A	XP_011540542.1:p.Phe274Tyr
XM_011542241.1:c.821T>A	XP_011540543.1:p.Phe274Tyr
XM_011542241.3:c.821T>A	XP_011540543.1:p.Phe274Tyr
XM_011542242.1:c.317T>A	XP_011540544.1:p.Phe106Tyr
XM_011542243.1:c.317T>A	XP_011540545.1:p.Phe106Tyr
XM_011542244.1:c.965T>A	XP_011540546.1:p.Phe322Tyr
XR_001737468.1:n.974T>A
XR_001737469.1:n.1844T>A
XR_001737470.1:n.974T>A
XR_002957738.1:n.974T>A
XR_241045.2:n.974T>A
XR_946776.1:n.974T>A
XR_946776.2:n.974T>A