Canonical Allele Identifier: CA2675871911
Gene: FBXO38 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148425546_148425559del , CM000667.2:g.148425546_148425559del GRCh38
NC_000005.9:g.147805109_147805122del , CM000667.1:g.147805109_147805122del GRCh37
NC_000005.8:g.147785302_147785315del NCBI36
NG_033871.1:g.46612_46625del

Transcript Alleles

HGVS Amino-acid change
ENST00000340253.10:c.1763_1776del MANE Select ENSP00000342023.6:p.Val588AspfsTer5
ENST00000296701.10:c.1763_1776del ENSP00000296701.6:p.Val588AspfsTer5
ENST00000340253.9:c.1763_1776del ENSP00000342023.5:p.Val588AspfsTer5
ENST00000394370.7:c.1763_1776del ENSP00000377895.3:p.Val588AspfsTer5
ENST00000513826.1:c.1763_1776del ENSP00000426410.1:p.Val588AspfsTer5
ENST00000514832.1:n.394_407del
NM_001271723.1:c.1763_1776del NP_001258652.1:p.Val588AspfsTer5
NM_030793.4:c.1763_1776del NP_110420.3:p.Val588AspfsTer5
XM_005268513.1:c.1763_1776del XP_005268570.1:p.Val588AspfsTer5
XM_006714797.1:c.1763_1776del XP_006714860.1:p.Val588AspfsTer5
XM_011537683.1:c.665_678del XP_011535985.1:p.Val222AspfsTer5
XM_011537684.1:c.563_576del XP_011535986.1:p.Val188AspfsTer5
NM_205836.2:c.1763_1776del NP_995308.1:p.Val588AspfsTer5
XM_006714797.2:c.1763_1776del XP_006714860.1:p.Val588AspfsTer5
XM_011537684.3:c.563_576del XP_011535986.1:p.Val188AspfsTer5
XM_017009899.1:c.665_678del XP_016865388.1:p.Val222AspfsTer5
XM_017009900.2:c.563_576del XP_016865389.1:p.Val188AspfsTer5
XM_017009901.2:c.665_678del XP_016865390.1:p.Val222AspfsTer5
XM_017009902.2:c.563_576del XP_016865391.1:p.Val188AspfsTer5
XM_024446223.1:c.1763_1776del XP_024301991.1:p.Val588AspfsTer5
XR_001742284.1:n.1909_1922del
NM_030793.5:c.1763_1776del NP_110420.3:p.Val588AspfsTer5
NM_205836.3:c.1763_1776del MANE Select NP_995308.1:p.Val588AspfsTer5
NM_001271723.2:c.1763_1776del NP_001258652.1:p.Val588AspfsTer5