Canonical Allele Identifier: CA1649907144
Gene: FBXL4 HGNC NCBI

Linked Data

dbSNP Id: rs1772779252

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.98926379_98926383del , CM000668.2:g.98926379_98926383del GRCh38
NC_000006.11:g.99374255_99374259del , CM000668.1:g.99374255_99374259del GRCh37
NC_000006.10:g.99480976_99480980del NCBI36
NG_033903.1:g.26627_26631del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369244.7:c.512+97_512+101del MANE Select ENSP00000358247.1:n.512+97_512+101del
ENST00000229971.2:c.512+97_512+101del ENSP00000229971.1:n.512+97_512+101del
ENST00000369244.6:c.512+97_512+101del ENSP00000358247.1:n.512+97_512+101del
NM_001278716.1:c.512+97_512+101del NP_001265645.1:n.512+97_512+101del
NM_012160.4:c.512+97_512+101del NP_036292.2:n.512+97_512+101del
NR_103836.1:n.903+97_903+101del
NR_103837.1:n.903+97_903+101del
XM_005266930.1:c.512+97_512+101del XP_005266987.1:n.512+97_512+101del
XM_011535748.1:c.512+97_512+101del XP_011534050.1:n.512+97_512+101del
XM_005266930.3:c.512+97_512+101del XP_005266987.1:n.512+97_512+101del
XM_011535748.3:c.512+97_512+101del XP_011534050.1:n.512+97_512+101del
XM_017010726.1:c.512+97_512+101del XP_016866215.1:n.512+97_512+101del
XM_017010727.2:c.512+97_512+101del XP_016866216.1:n.512+97_512+101del
XM_017010728.1:c.-291+97_-291+101del XP_016866217.1:n.-291+97_-291+101del
NM_001278716.2:c.512+97_512+101del MANE Select NP_001265645.1:n.512+97_512+101del
NR_103836.2:n.843+97_843+101del
NR_103837.2:n.843+97_843+101del
NM_012160.5:c.512+97_512+101del NP_036292.2:n.512+97_512+101del