Canonical Allele Identifier: CA2675871881
Gene: FBXO38 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148425460del , CM000667.2:g.148425460del GRCh38
NC_000005.9:g.147805023del , CM000667.1:g.147805023del GRCh37
NC_000005.8:g.147785216del NCBI36
NG_033871.1:g.46526del

Transcript Alleles

HGVS Amino-acid change
ENST00000340253.10:c.1739-62del MANE Select ENSP00000342023.6:n.1739-62del
ENST00000296701.10:c.1739-62del ENSP00000296701.6:n.1739-62del
ENST00000340253.9:c.1739-62del ENSP00000342023.5:n.1739-62del
ENST00000394370.7:c.1739-62del ENSP00000377895.3:n.1739-62del
ENST00000513826.1:c.1739-62del ENSP00000426410.1:n.1739-62del
ENST00000514832.1:n.370-62del
NM_001271723.1:c.1739-62del NP_001258652.1:n.1739-62del
NM_030793.4:c.1739-62del NP_110420.3:n.1739-62del
XM_005268513.1:c.1739-62del XP_005268570.1:n.1739-62del
XM_006714797.1:c.1739-62del XP_006714860.1:n.1739-62del
XM_011537683.1:c.641-62del XP_011535985.1:n.641-62del
XM_011537684.1:c.539-62del XP_011535986.1:n.539-62del
NM_205836.2:c.1739-62del NP_995308.1:n.1739-62del
XM_006714797.2:c.1739-62del XP_006714860.1:n.1739-62del
XM_011537684.3:c.539-62del XP_011535986.1:n.539-62del
XM_017009899.1:c.641-62del XP_016865388.1:n.641-62del
XM_017009900.2:c.539-62del XP_016865389.1:n.539-62del
XM_017009901.2:c.641-62del XP_016865390.1:n.641-62del
XM_017009902.2:c.539-62del XP_016865391.1:n.539-62del
XM_024446223.1:c.1739-62del XP_024301991.1:n.1739-62del
XR_001742284.1:n.1885-62del
NM_030793.5:c.1739-62del NP_110420.3:n.1739-62del
NM_205836.3:c.1739-62del MANE Select NP_995308.1:n.1739-62del
NM_001271723.2:c.1739-62del NP_001258652.1:n.1739-62del