Canonical Allele Identifier: CA2675871914

Gene: FBXO38

Linked Data

• gnomAD v4: 5-148425561-TTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148425562_148425563del , CM000667.2:g.148425562_148425563del	GRCh38
NC_000005.9:g.147805125_147805126del , CM000667.1:g.147805125_147805126del	GRCh37
NC_000005.8:g.147785318_147785319del	NCBI36
NG_033871.1:g.46628_46629del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340253.10:c.1779_1780del MANE Select	ENSP00000342023.6:p.Thr594CysfsTer3
ENST00000296701.10:c.1779_1780del	ENSP00000296701.6:p.Thr594CysfsTer3
ENST00000340253.9:c.1779_1780del	ENSP00000342023.5:p.Thr594CysfsTer3
ENST00000394370.7:c.1779_1780del	ENSP00000377895.3:p.Thr594CysfsTer3
ENST00000513826.1:c.1779_1780del	ENSP00000426410.1:p.Thr594CysfsTer3
ENST00000514832.1:n.410_411del
NM_001271723.1:c.1779_1780del	NP_001258652.1:p.Thr594CysfsTer3
NM_030793.4:c.1779_1780del	NP_110420.3:p.Thr594CysfsTer3
XM_005268513.1:c.1779_1780del	XP_005268570.1:p.Thr594CysfsTer3
XM_006714797.1:c.1779_1780del	XP_006714860.1:p.Thr594CysfsTer3
XM_011537683.1:c.681_682del	XP_011535985.1:p.Thr228CysfsTer3
XM_011537684.1:c.579_580del	XP_011535986.1:p.Thr194CysfsTer3
NM_205836.2:c.1779_1780del	NP_995308.1:p.Thr594CysfsTer3
XM_006714797.2:c.1779_1780del	XP_006714860.1:p.Thr594CysfsTer3
XM_011537684.3:c.579_580del	XP_011535986.1:p.Thr194CysfsTer3
XM_017009899.1:c.681_682del	XP_016865388.1:p.Thr228CysfsTer3
XM_017009900.2:c.579_580del	XP_016865389.1:p.Thr194CysfsTer3
XM_017009901.2:c.681_682del	XP_016865390.1:p.Thr228CysfsTer3
XM_017009902.2:c.579_580del	XP_016865391.1:p.Thr194CysfsTer3
XM_024446223.1:c.1779_1780del	XP_024301991.1:p.Thr594CysfsTer3
XR_001742284.1:n.1925_1926del
NM_030793.5:c.1779_1780del	NP_110420.3:p.Thr594CysfsTer3
NM_205836.3:c.1779_1780del MANE Select	NP_995308.1:p.Thr594CysfsTer3
NM_001271723.2:c.1779_1780del	NP_001258652.1:p.Thr594CysfsTer3