Canonical Allele Identifier: CA2675871921
Gene: FBXO38 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148425624_148425642del , CM000667.2:g.148425624_148425642del GRCh38
NC_000005.9:g.147805187_147805205del , CM000667.1:g.147805187_147805205del GRCh37
NC_000005.8:g.147785380_147785398del NCBI36
NG_033871.1:g.46690_46708del

Transcript Alleles

HGVS Amino-acid Change
ENST00000340253.10:c.1841_1859del MANE Select ENSP00000342023.6:p.Ile614SerfsTer21
ENST00000296701.10:c.1841_1859del ENSP00000296701.6:p.Ile614SerfsTer22
ENST00000340253.9:c.1841_1859del ENSP00000342023.5:p.Ile614SerfsTer21
ENST00000394370.7:c.1841_1859del ENSP00000377895.3:p.Ile614SerfsTer21
ENST00000513826.1:c.1841_1859del ENSP00000426410.1:p.Ile614SerfsTer22
ENST00000514832.1:n.472_490del
NM_001271723.1:c.1841_1859del NP_001258652.1:p.Ile614SerfsTer22
NM_030793.4:c.1841_1859del NP_110420.3:p.Ile614SerfsTer21
XM_005268513.1:c.1841_1859del XP_005268570.1:p.Ile614SerfsTer21
XM_006714797.1:c.1841_1859del XP_006714860.1:p.Ile614SerfsTer21
XM_011537683.1:c.743_761del XP_011535985.1:p.Ile248SerfsTer21
XM_011537684.1:c.641_659del XP_011535986.1:p.Ile214SerfsTer21
NM_205836.2:c.1841_1859del NP_995308.1:p.Ile614SerfsTer21
XM_006714797.2:c.1841_1859del XP_006714860.1:p.Ile614SerfsTer21
XM_011537684.3:c.641_659del XP_011535986.1:p.Ile214SerfsTer21
XM_017009899.1:c.743_761del XP_016865388.1:p.Ile248SerfsTer21
XM_017009900.2:c.641_659del XP_016865389.1:p.Ile214SerfsTer21
XM_017009901.2:c.743_761del XP_016865390.1:p.Ile248SerfsTer21
XM_017009902.2:c.641_659del XP_016865391.1:p.Ile214SerfsTer21
XM_024446223.1:c.1841_1859del XP_024301991.1:p.Ile614SerfsTer21
XR_001742284.1:n.1987_2005del
NM_030793.5:c.1841_1859del NP_110420.3:p.Ile614SerfsTer21
NM_205836.3:c.1841_1859del MANE Select NP_995308.1:p.Ile614SerfsTer21
NM_001271723.2:c.1841_1859del NP_001258652.1:p.Ile614SerfsTer22