Canonical Allele Identifier: CA2675871916
Gene: FBXO38 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148425567_148425568insGG , CM000667.2:g.148425567_148425568insGG GRCh38
NC_000005.9:g.147805130_147805131insGG , CM000667.1:g.147805130_147805131insGG GRCh37
NC_000005.8:g.147785323_147785324insGG NCBI36
NG_033871.1:g.46633_46634insGG

Transcript Alleles

HGVS Amino-acid change
ENST00000340253.10:c.1784_1785insGG MANE Select ENSP00000342023.6:p.His596ValfsTer13
ENST00000296701.10:c.1784_1785insGG ENSP00000296701.6:p.His596ValfsTer13
ENST00000340253.9:c.1784_1785insGG ENSP00000342023.5:p.His596ValfsTer13
ENST00000394370.7:c.1784_1785insGG ENSP00000377895.3:p.His596ValfsTer13
ENST00000513826.1:c.1784_1785insGG ENSP00000426410.1:p.His596ValfsTer13
ENST00000514832.1:n.415_416insGG
NM_001271723.1:c.1784_1785insGG NP_001258652.1:p.His596ValfsTer13
NM_030793.4:c.1784_1785insGG NP_110420.3:p.His596ValfsTer13
XM_005268513.1:c.1784_1785insGG XP_005268570.1:p.His596ValfsTer13
XM_006714797.1:c.1784_1785insGG XP_006714860.1:p.His596ValfsTer13
XM_011537683.1:c.686_687insGG XP_011535985.1:p.His230ValfsTer13
XM_011537684.1:c.584_585insGG XP_011535986.1:p.His196ValfsTer13
NM_205836.2:c.1784_1785insGG NP_995308.1:p.His596ValfsTer13
XM_006714797.2:c.1784_1785insGG XP_006714860.1:p.His596ValfsTer13
XM_011537684.3:c.584_585insGG XP_011535986.1:p.His196ValfsTer13
XM_017009899.1:c.686_687insGG XP_016865388.1:p.His230ValfsTer13
XM_017009900.2:c.584_585insGG XP_016865389.1:p.His196ValfsTer13
XM_017009901.2:c.686_687insGG XP_016865390.1:p.His230ValfsTer13
XM_017009902.2:c.584_585insGG XP_016865391.1:p.His196ValfsTer13
XM_024446223.1:c.1784_1785insGG XP_024301991.1:p.His596ValfsTer13
XR_001742284.1:n.1930_1931insGG
NM_030793.5:c.1784_1785insGG NP_110420.3:p.His596ValfsTer13
NM_205836.3:c.1784_1785insGG MANE Select NP_995308.1:p.His596ValfsTer13
NM_001271723.2:c.1784_1785insGG NP_001258652.1:p.His596ValfsTer13