Canonical Allele Identifier: CA2679757505
Gene: FBXL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98874206_98874208del , CM000668.2:g.98874206_98874208del GRCh38
NC_000006.11:g.99322082_99322084del , CM000668.1:g.99322082_99322084del GRCh37
NC_000006.10:g.99428803_99428805del NCBI36
NG_033903.1:g.78801_78803del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.*72_*74del MANE Select ENSP00000358247.1:n.*72_*74del
ENST00000229971.2:c.*72_*74del ENSP00000229971.1:n.*72_*74del
ENST00000369244.6:c.*72_*74del ENSP00000358247.1:n.*72_*74del
NM_001278716.1:c.*72_*74del NP_001265645.1:n.*72_*74del
NM_012160.4:c.*72_*74del NP_036292.2:n.*72_*74del
NR_103836.1:n.1983_1985del
XM_005266930.1:c.*72_*74del XP_005266987.1:n.*72_*74del
XM_005266930.3:c.*72_*74del XP_005266987.1:n.*72_*74del
XM_017010726.1:c.*72_*74del XP_016866215.1:n.*72_*74del
XM_017010727.2:c.*72_*74del XP_016866216.1:n.*72_*74del
XM_017010728.1:c.*72_*74del XP_016866217.1:n.*72_*74del
NM_001278716.2:c.*72_*74del MANE Select NP_001265645.1:n.*72_*74del
NR_103836.2:n.1923_1925del
NM_012160.5:c.*72_*74del NP_036292.2:n.*72_*74del